DIN 50014

Climates and their technical application; standard atmospheres

DIN 38411-1

German standard methods for the examination of water, waste water and sludge; Microbiological methods (Group K); Preparation for the microbiological examination of water samples (K1)

DIN 50008-1

Atmospheres and their technical application; Standard atmospheres over aqueous solutions; Saturated salt solutions, glycerol solutions

DIN 50010-2

Climates and their technical application; climatological terms and definitions; physical terms and definitions

DIN EN 14375 Berichtigung 1

Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing; Corrigenda to DIN EN 14375:2004-02

DIN EN ISO 7439

Copper-bearing intra-uterine contraceptive devices - Requirements, tests (ISO 7439:2002)

DIN 10102

Microbiological analysis of meat and meat products; detection of clostridium botulinum and botulinum toxin

DIN 10115

Principles of detecting and determining microorganisms in foodstuffs using impedance methods

DIN 10118

Analysis of foodstuffs - Detection of verotoxine-forming Escherichia (E.) coli-strains (VTEC) in food derived from animals

DIN 10120

Detecting Salmonella in foodstuffs using impedance methods

DIN 10121

Detection of salmonella in foodstuffs by enzyme-linked fluorescent immunoassay

DIN 10135

Method of detecting Salmonella using the polymerase chain reaction (PCR)

DIN 10163-2

Microbiological examination of meat and meat products; determination of coagulase-positive staphylococci; by the drop method

DIN 10164-1

Microbiological examination of meat and meat products; determination of Enterobacteriaceae by the spatula method (reference method)

DIN 10164-2

Microbiological examination of meat and meat products; determination of Enterobacteriaceae by the drop method

DIN 10167

Detection of Escherichia coli O 157 in meat and meat products

DIN 10182-2

Microbiological analysis of milk; detection of inhibitors in milk; routine method (brilliant black reduction test)

DIN 10194

Microbiological analysis of milk; detection of Streptococcus agalactiae in untreated milk

DIN 10198-1

Determining presumptive Bacillus cereus in milk by colony count at 37 °C

DIN 1304-2

Letter symbols for physical quantities - Symbols for use in meteorology and geophysics

DIN 1310

Composition of (gaseous, liquid and solid) mixtures; concepts, symbols

DIN 1312

Geometrical Orientation

DIN 1314

Pressure; Basic Definitions, Units

DIN 13902-1

Dentistry - Terminology of oral implantology - Part 1: Endosseous dental implant systems

DIN 19650

Hygiene parameters for irrigation water

DIN 38411-6

German standard methodes for the examination of water, waste water und sludge; microbiological methods (group K); determination of Escherichia coli and coliform organisms (K6)

DIN 38411-8

German standard methods for the analysis of water, waste water and sludge; Microbiological methods (group K); Detection of Pseudomonas aeruginosa (K8)

DIN 38411-9

German standard methods for the examination of water, waste water and sludge - Microbiological methods (group K) - Part 9: Determination of enterobacterial common antigen (ECA) for the detection of lactose-fermenting enterobacteriaceae (K 9)

DIN 38412-48

German standard methods for the examination of water, waste water and sludge - Bio-assays (group L) - Part 48: Arthrobacter globiformis toxicity test for polluted solid material (L 48)

DIN 50008-2

Atmospheres and their technical application; Standard atmospheres over aqueous solutions; Sulfuric acid solutions

DIN 50010-1

Climates and Their Technical Application; Climatic Concepts; General Climatic Concepts

DIN 50012-1

Climates and their technical application; methods of measuring humidity; general

DIN 50012-2

Climates and their technical application; methods of measuring humidity; psychrometers

DIN 50012-3

Climates and their technical application; methods of measuring humidity; hair hygrometer

DIN 50012-4

Climates and their technical application; methods of measuring humidity; dew point hygrometer

DIN 50012-5

Artificial climates in technical applications; methods of measuring humidity; LiCl -hygrometers

DIN 50015

Atmospheres and their Technical Application; Constant Test Atmospheres

DIN 58369

Transfusion, infusion - Disposable hanging devices for bottles for transfusion and infusion - Requirements, test

DIN 58901-1

Haemostaseology - Determination of factor VII coagulant activity (F VII C) - Part 1: Reference measurement procedure for the one-stage method

DIN 58901-2

Haemostaseology - Determination of factor VII coagulant activity (F VII C) - Part 2: Reference measurement procedure using a synthetic peptide substrate

DIN 58902

Haemostaseology - Reference measurement procedure for the determination of batroxobin time

DIN 58903

Haemostaseology - Deficient plasma - Requirements, preparation

DIN 58904

Haemostaseology - Determination of protein C activity - Reference measurement procedure with a chromogenic peptide substrate

DIN 58905-1

Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing

DIN 58906-1

Haemostaseology - Determination of fibrinogen concentration - Part 1: Reference measurement procedure for the determination of clottable fibrinogen as described by Clauss

DIN 58907-1

Haemostaseology - Determination of factor IX coagulant activity (F IX C) - Part 1: Reference measurement procedure for the one-stage method

DIN 58908

Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure

DIN 58909-1

Haemostaseology - Determination of factor VIII coagulant activity (F VIII C) - Part 1: Reference measurement procedure for the one-stage method

DIN 58909-2

Haemostaseology - Determination of factor VIII coagulant activity (F VIII C) - Part 2: Reference measurement procedure using a synthetic peptide substrate

DIN 58910-1

Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood

DIN 58910-2

Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood

DIN 58910-3

Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood

DIN 58910-4

Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood

DIN 58911-1

Haemostaseology - Calibration of measurement procedures - Part 1: Clotting time measurement procedures

DIN 58911-2

Haemostaseology - Calibration of measurement procedures - Part 2: Photometric measurement procedures

DIN 58912-1

Haemostaseology - Determination of the antithrombin III activity - Part 1: Reference measurement procedure using a synthetic peptide substrate

DIN 58913-1

Haemostaseology - Determination of factor II coagulant activity (F II C) and factor X coagulant activity (F X C) - Part 1: Reference measurement procedure for the one-stage method

DIN 58914-1

Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood

DIN 58930

Haemostaseology - INR calibration plasmas - Requirements, preparation and use

DIN 58932-4

Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes

DIN 58939-1

Haemostaseology - Reference plasma - Part 1: Requirements, preparation

DIN 58940-1

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 1: Terminology

DIN 58940-10 Beiblatt 1

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 10: Criteria for the evaluation of the in vitro efficacy of new antimicrobial agents; Supplement 1: Data form sheets

DIN 58940-2 Beiblatt 2

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 2: Active substance carriers for the agar diffusion test; Carrier loads and values required for drawing a standard curve

DIN 58940-20

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 20: Codes for antimicrobial agents

DIN 58940-20 Beiblatt 1

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 20: Coding of antimicrobial agents - Codes for antimicrobial agents

DIN 58940-3 Beiblatt 1

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 3: Agar diffusion test; data for the interpretation of inhibition zone diameters

DIN 58940-4

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 4: Evaluation classes of the minimum inhibitory concentration

DIN 58940-8

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 8: Microdilution; General method-specific requirements

DIN 58940-81

Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 81: Microdilution; Special requirements for testing of non-fastidious bacteria

DIN 58940-82

Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 82: Microdilution; Special requirements for testing of fastidious bacteria

DIN 58940-83

Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 83: Microdilution; Special requirements for testing of strictly anaerobically bacteria

DIN 58940-84

Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 84: Microdilution; Special requirements for testing of fungi against antifungal agents

DIN 58942-2

Medical microbiology - Culture media - Part 2: Ready-to-use blood culture systems

DIN 58942-3

Medical microbiology - Culture media - Part 3: Dip slides for microbiological urine analysis

DIN 58942-4

Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria

DIN 58942-4 Beiblatt 1

Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria - Systems, media and conditions for the transport of selected pathogens in clinical specimens

DIN 58942-5

Medical microbiology - Culture media - Part 5: Requirements and selection of culture media for the diagnostic of stool specimen

DIN 58943 Beiblatt 1

Medical microbiology - Diagnosis of tuberculosis - Guidance for the specialized use of methods of detection

DIN 58943-40

Medical microbiology - Diagnosis of tuberculosis - Part 40: Evaluation criteria for fast culture procedures for the detection of mycobacteria

DIN 58943-8

Medical microbiology - Diagnosis of tuberculosis - Part 8: Methods for the determination of susceptibility of tubercle bacilli to chemotherapeutic agents

DIN 58959 Beiblatt 1

Quality management in medical microbiology - Overview and index

DIN 58959-1

Quality management in medical microbiology - Part 1: Requirements for the QM system

DIN 58959-10

Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials

DIN 58959-10 Beiblatt 1

Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials; control strains for commonly used materials

DIN 58959-11

Quality management in medical microbiology - Part 11: Requirements for the use of control material for testing ready-to-use tests and test kits

DIN 58959-12

Quality management in medical microbiology - Part 12: Requirements for the use of control material for testing immunological reagent kits

DIN 58959-12 Beiblatt 1

Quality management in medical microbiology - Part 12: Requirements for the use of control material for testing immunological reagent kits; control material for commonly used immune diagnostics

DIN 58959-13

Quality management in medical microbiology - Part 13: Criteria for determination of active substance breakpoint for control strains used in susceptibility testing

DIN 58959-14

Quality management in medical microbiology - Part 14: Requirements for the use of control strains for susceptibility testing of aerobic bacteria

DIN 58959-14 Beiblatt 1

Quality management in medical microbiology - Part 14: Requirements for the use of control strains for susceptibility testing of aerobic bacteria; MIC/IZD limits for aerobes

DIN 58959-15

Quality management in medical microbiology Part 15: Requirements for the use of control strains for susceptibility testing of anaerobic bacteria

DIN 58959-15 Beiblatt 1

Quality management in medical microbiology - Part 15: Requirements for the use of control strains for susceptibility testing of anaerobic bacteria; MIC/IZD limits for anaerobes

DIN 58959-16

Quality management in medical microbiology - Part 16: Requirements for the use of control strains for susceptibility testing of special bacteria

DIN 58959-17

Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria

DIN 58959-17 Beiblatt 1

Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria; control strains for commonly used culture media, reagents and test

DIN 58959-18

Quality management in medical microbiology - Part 18: Requirements for the use of control strains for the examination of mycoplasms

DIN 58959-18 Beiblatt 1

Quality management in medical microbiology - Part 18: Requirements for the use of control strains for the examination of mycoplasms; control strains for commonly used culture media and reagents

DIN 58959-19

Quality management in medical microbiology - Part 19: Requirements for the use of control strains for the examination of fungi

DIN 58959-19 Beiblatt 1

Quality management in medical microbiology - Part 19: Requirements for the use of control strains for the examination of fungi; control strains for commonly used culture media and reagents

DIN 58959-2

Quality management in medical microbiology - Part 2: Requirements for sample collection, transport and acceptance of specimens

DIN 58959-2 Beiblatt 1

Quality management in medical microbiology - Part 2: Requirements for sample collection, transport and acception of specimens; characteristics for special specimens

DIN 58959-20

Quality management in medical microbiology - Part 20: Requirements for the use of control material for the examination of protozoae and microorganisms of higher order

DIN 58959-3

Quality management in medical microbiology - Part 3: Requirements for request and report forms

DIN 58959-4

Quality management in medical microbiology - Part 4: Requirements for investigations using light microscopes

DIN 58959-6

Quality management in medical microbiology - Part 6: Requirements for control strains

DIN 58959-6 Beiblatt 1

Quality management in medical microbiology - Part 6: Requirements for control strains; examples for production and preservation of bacteria used as stock cultures and working cultures

DIN 58959-6 Beiblatt 2

Quality management in medical microbiology - Part 6: Requirements for control strains; examples for production and preservation of fungi used as stock cultures and working cultures

DIN 58959-7

Quality management in medical microbiology - Part 7: General requirements for the use of control strains

DIN 58959-7 Beiblatt 1

Quality management in medical microbiology - Part 7: General requirements for the use of control strains; sources of supply for control strains

DIN 58959-7 Beiblatt 2

Quality management in medical microbiology - Part 7: General requirements for the use of control strains; ATTC and DSM numbers of commonly used control strains

DIN 58959-7 Beiblatt 3

Quality management in medical microbiology - Part 7: General requirements for the use of control strains; examples for control cards documentation of test results

DIN 58959-8

Quality management in medical microbiology - Part 8: Requirements for the use of control strains for testing swabs, transport media, media of dip-slides, and blood culture media

DIN 58959-9

Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media

DIN 58959-9 Beiblatt 1

Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media; control strains for commonly used culture media

DIN 58959-9 Beiblatt 2

Quality management in medical microbiology - Part 9: Requirements for the use of control strains for testing culture media; maximum storage times for ready to use culture media

DIN 58967-10

Serodiagnosis of infectious diseases and diseases of the immune system; part 10: concepts, general requirements

DIN 58967-20

Medical microbiology and immunology - Diagnostics of infectious diseases and diseases of the immune system in serology and molecular biology - Part 20: General method-specific requirements for immunofluorescence tests (IFT)

DIN 58967-30

Diagnostics of infectious diseases and diseases of the immune systems in serological and molecularbiology - Part 30: ELISA (Enzyme-Linked-Immuno-Sorbent-Assay); terms, general method-specific requirements

DIN 58967-40

Serodiagnosis of infectious diseases and diseases of the immune system; immunoblot (IB); part 40: terms, general method-specific requirements

DIN 58967-60

Diagnostics of infectious deseases and deseases of the immune system in serology and molecular biology - Part 60: Polymerase chain reaction (PCR); Terminology, general method-specific requirements

DIN 58969-10

Medical microbiology - Diagnostics of infectious diseases in serological and molecular biology - Part 10: Complement fixation test (CFT)

DIN 58969-41

Medical microbiology; serodiagnosis of infectious diseases; immunoblot (IB); part 41: special requirements for the detection of antibodies against Human Immunodeficiency Virus HIV-1 or HIV-2

DIN 58969-44

Medical microbiology - Diagnostics of infectious diseases in serology and molecular biology - Part 44: Immunoblot (IB); Special requirements for the detection of antibodies against Borrelia burgdorferi

DIN 58969-61

Medical microbiology - Serodiagnosis of infectious diseases - Part 61: Polymerase chain reaction (PCR); special requirements for the detection of nucleic acid sequences of the Human Immunodeficiency Viruses HIV-1 and HIV-2

DIN 58969-62

Medical microbiology - Diagnosis of infectious diseases in serology and molecular biology - Part 62: Polymerase chain reaction (PCR); Special requirements for the detection of nucleic acid sequences of the mycobacterium tuberculosis complex (MTC)

DIN 58985

Laboratory medicine - Decision-marking criteria

DIN EN 12181

Oropharyngeal airways; German version EN 12181:1998

DIN EN 12225

Geotextiles and geotextile-related products - Method for determining the microbiological resistance by a soil burial test; German version EN 12225:2000

DIN EN 12322

In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media; German version EN 12322:1999

DIN EN 12442-3

Animal tissue and their derivatives utilized in the manufacture of medical devices - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible agents; English version of DIN EN 12442-3

DIN EN 12469

Biotechnology - Performance criteria for microbiological safety cabinets; English version of DIN EN 12469

DIN EN 12780

Water quality - Detection and enumeration of Pseudomonas aeruginosa by membrane filtration

DIN EN 868-3

Packaging materials and systems for medical devices which are to be sterilized - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods

DIN EN 868-7

Packaging materials and systems for medical devices which are to be sterilized - Part 7: Adhesive coated paper for the manufacture of heat sealable packs for medical use for sterilization by ethylene oxide or irradiation - Requirements and test methods

DIN EN 980

Graphical symbols for use in the labelling of medical devices

DIN EN ISO 11138-2

Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006)

DIN EN ISO 17510-1

Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy devices (ISO 17510-1:2002)

DIN EN ISO 18472

Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2006)

DIN EN ISO 6360-1

Dentistry - Number coding system for rotary instruments - Part 1: General characteristics (ISO 6360-1:2004)

DIN ISO 15473

Soil quality - Guidance on laboratory testing for biodegradation of organic chemicals in soil under anaerobic conditions (ISO 15473:2002)

DIN 13902-3

(DRAFT) Dentistry - Terminology of oral implantology - Part 3: Clinical terms

DIN 58932-5

(DRAFT) Haematology - Determination of the concentration of blood corpuscles in blood - Part 5: Reference method for the determination of the concentration of thrombocytes

DIN CEN/TS 14463

Health informatics - A syntax to represent the content of medical classification systems (ClaML); German version CEN/TS 14463:2003, English texts

DIN CWA 14445

European Generic Article Register - Recommendations regarding terminology of product groups and article designations and relation to other nomenclatures; English version CWA 14445:2002

DIN CWA 14446

European Generic Article Register - Conceptual description of EGAR, working methodology and relation to the tendering and procurement process in the healthcare sector; English version CWA 14446:2002

DIN EN 1040

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics - Test method and requirements (phase 1)

DIN EN 1041

Medical devices - Information supplied by the manufacturer

DIN EN 1060-1

Non-invasive sphygmomanometers - General requirements

DIN EN 1060-1/A1

Non-invasive sphygmomanometers - Part 1: General requirements; Amendment A1

DIN EN 1060-2

Non-invasive sphygmomanometers - Supplementary requirements for mechanical sphygmomanometers

DIN EN 1060-3

Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

DIN EN 1060-4

Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers

DIN EN 12006-2

Non-active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits; German version EN 12006-2:1998

DIN EN 12006-3

Non-active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices

DIN EN 12010

Non-active surgical implants - Joint replacement implants - Particular requirements; German version EN 12010:1997

DIN EN 12011

Instrumentation to be used in association with non-active surgical implants - General requirements

DIN EN 12022

Blood gas exchangers

DIN EN 12128

Biotechnology - Laboratories for research, development and analysis - Containment levels of microbiology laboratories, areas of risk, localities and physical safety requirements; German version EN 12128:1998

DIN EN 12181

Oropharyngeal airways

DIN EN 12182

Technical aids for disabled persons - General requirements and test methods

DIN EN 12183

Manually propelled wheelchairs - Requirements and test methods

DIN EN 12184

Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods

DIN EN 12225

Geotextiles and geotextile-related products - Method for determining the microbiological resistance by a soil burial test; English version of DIN EN 12225

DIN EN 12286

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures

DIN EN 12287

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials

DIN EN 12296

Biotechnology - Equipment - Guidance on testing procedures for cleanability; German version EN 12296:1998

DIN EN 12297

Biotechnology - Equipment - Guidance on testing procedures for sterilizability; German version EN 12297:1998

DIN EN 12298

Biotechnology - Equipment - Guidance on procedures for testing leaktightness; German version EN 12298:1998

DIN EN 12305

Biotechnology - Modified organisms for application in the environment - Guidance for the sampling strategies for deliberate releases of genetically modified plants

DIN EN 12306

Biotechnology - Guidance for quality control of diagnostic kits used in agriculture, plant and animal pest and disease control and environmental contamination

DIN EN 12307

Biotechnology - Large-scale process and production - Guidance for good practice, procedures, training and control for personnel

DIN EN 12342

Breathing tubes intended for use with anaesthetic apparatus and ventilators

DIN EN 12342

Breathing tubes intended for use with anaesthetic apparatus and ventilators; German version EN 12342:1998

DIN EN 12347

Biotechnology - Performance criteria for steam sterilizers and autoclaves

DIN EN 12353

Chemical disinfectants and antiseptics - Preservation of microbial strains used for the determination of bactericidal and fungicidal activity

DIN EN 12353

Chemical disinfectants and antiseptics - Preservation of test organisms used for the determination of bactericidal, mycobactericidal, sporicidal and fungicidal activity

DIN EN 12439

Steril rectal catheters for single use

DIN EN 12442-1

Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 1: Analysis and management of risk; English version of DIN EN 12442-1

DIN EN 12442-2

Animal tissues and their derivatives utilized in the manufacture of medical devices - Part 2: Controls on sourcing, collection and handling; English version of DIN EN 12442-2

DIN EN 12460

Biotechnology - Large-scale process and production - Guidance on equipment selection and installation in accordance with the biological risk

DIN EN 12461

Biotechnology - Large-scale process and production - Guidance for the handling, inactivating and testing of waste

DIN EN 12462

Biotechnology - Performance criteria for pumps

DIN EN 12468

Biotechnology - Modified organisms for application in the environment - Guidance for the monitoring strategies for deliberate releases of genetically modified plants; German version EN 12468:1997

DIN EN 12531

Castors and wheels - Hospital bed castors

DIN EN 12563

Non-active surgical implants - Joint replacement implants - Specific requirements for hip joint replacement implants

DIN EN 12564

Non-active surgical implants - Joint replacement implants - Specific requirements for knee joint replacement implants

DIN EN 12682

Biotechnology - Modified organisms for application in the environment - Guidance for the characterization of the genetically modified organism by analysis of the functional expression of the genomic modification

DIN EN 12683

Biotechnology - Modified organisms for application in the environment - Guidance for the characterization of the genetically modified organism by analysis of the molecular stability of the genomic modification

DIN EN 12685

Biotechnology - Modified organisms for application in the environment - Guidance for the monitoring strategies for deliberate releases of genetically modified microorganisms, including viruses

DIN EN 12686

Biotechnology - Modified organisms for application in the environment - Guidance for the sampling strategies for deliberate releases of genetically modified microorganisms, including viruses

DIN EN 12687

Biotechnology - Modified organisms for application in the environment - Guidance for the characterization of the genetically modified organism by analysis of the genomic modification

DIN EN 12689

Biotechnology - Guidance on assessment of the purity, biological activity and stability of microorganism based products

DIN EN 12690

Biotechnology - Performance criteria for shaft seals

DIN EN 12738

Biotechnology - Laboratories for research, development and analysis - Guidance for containment of animals inoculated with microorganisms in experiments

DIN EN 12740

Biotechnology - Laboratories for research, development and analysis - Guidance for handling, inactivating and testing of waste

DIN EN 12741

Biotechnology - Laboratories for research, development and analysis - Guidance for biotechnology laboratory operations

DIN EN 1275

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of basic fungicidal or basic yeasticidal activity of chemical disinfectants and antiseptics - Test method and requirements (phase 1)

DIN EN 1276

Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic, and institutional areas - Test method and requirements (phase 2, step 1)

DIN EN 12791

Chemical disinfectants and antiseptics - Surgical hand disinfection - Test method and requirement (phase 2/step 2)

DIN EN 1281-2

Anaesthetic and respiratory equipment - Threaded weight-bearing conical connectors (ISO 5356-2:1987, modified)

DIN EN 1282-2

Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)

DIN EN 1283

Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits

DIN EN 12884

Biotechnology - Performance criteria for centrifuges

DIN EN 12885

Biotechnology - Performance criteria for cell disrupters

DIN EN 13014

Connections for gas sampling tubes to anaesthetic and respiratory equipment; English version of DIN EN 13014

DIN EN 13060

Small steam sterilizers

DIN EN 13091

Biotechnology - Performance criterai for filter elements and filtration assemblies; English version of DIN EN 13091

DIN EN 13092

Biotechnology - Equipment - Guidance on sampling and inoculation procedures; English version of DIN EN 13092

DIN EN 13095

Biotechnology - Performance criteria for off-gas systems; English version of DIN EN 13095

DIN EN 13098

Workplace atmospheres - Guidelines for measurement of airborne micro-organisms and endotoxin; English version of DIN EN 13098

DIN EN 13204

Double acting hydraulic rescue tools for fire and rescue service use - Safety and performance requirements

DIN EN 13220

Flow-metering devices for connection to terminal units of medical gas pipeline systems

DIN EN 13311-1

Biotechnology - Performance criteria for vessels - Part 1: General performance criteria; English version of DIN EN 13311-1

DIN EN 13311-2

Biotechnology - Performance criteria for vessels - Part 2: Pressure protection devices; English version of DIN EN 13311-2

DIN EN 13311-3

Biotechnology - Performance criteria for vessels - Part 3: Glass pressure vessels; English version of DIN EN 13311-3

DIN EN 13311-4

Biotechnology - Performance criteria for vessels - Part 4: Bioreactors; English version of DIN EN 13311-4

DIN EN 13311-5

Biotechnology - Performance criteria for vessels - Part 5: Kill tanks; English version of DIN EN 13311-5

DIN EN 13311-6

Biotechnology - Performance criteria for vessels - Part 6: Chromatography columns; English version of DIN EN 13311-6

DIN EN 13312-1

Biotechnology - Performance criteria for piping and instrumentation - Part 1: General performance criteria; English version of DIN EN 13312-1

DIN EN 13312-2

Biotechnology - Performance criteria for piping and instrumentation - Part 2: Couplings; English version of DIN EN 13312-2

DIN EN 13312-3

Biotechnology - Performance criteria for piping and instrumentation - Part 3: Sampling and inoculation devices; English version of DIN EN 13312-3

DIN EN 13312-4

Biotechnology - Performance criteria for piping and instrumentation - Part 4: Tubes and pipes; English version of DIN EN 13312-4

DIN EN 13312-5

Biotechnology - Performance criteria for piping and instrumentation - Part 5: Valves; English version of DIN EN 13312-5

DIN EN 13312-6

Biotechnology - Performance criteria for piping and instrumentation - Part 6: Equipment probes; English version of DIN EN 13312-6

DIN EN 13328-1

Breathing system filters for anaesthetic and respiratory use - Part 1: Salt test method to assess filtration performance

DIN EN 13328-2

Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (includes Amendment A1:2003)

DIN EN 13441

Biotechnology - Laboratories for research, development and analysis - Guidance on containment of genetically modifies plants

DIN EN 13503-6

Ophthalmic implants - Intraocular lenses - Part 6: Shelf-life and transport stability (ISO 11979-6:2002, modified)

DIN EN 13532

General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts

DIN EN 13544-1

Respiratory therapy equipment - Part 1: Nebulizing systems and their components (includes Amendment A1:2004)

DIN EN 13544-2

Respiratory therapy equipment - Part 2: Tubing and connectors

DIN EN 13544-3

Respiratory therapy equipment - Part 3: Air entrainment devices; English version of DIN EN 13544-3

DIN EN 13610

Quantitative suspension test for the evaluation of virucidal activity against bacteriophages of chemical disinfectants used in food and industrial areas - Test method and requirements (phase 2, step 1);

DIN EN 13612

Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts

DIN EN 13624

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)

DIN EN 13640

Stability testing of in vitro diagnostic reagent; German version EN 13640:2002, German and English texts

DIN EN 13641

Elimination or reduction of risk of infection related to in vitro diagnostic reagents; German version EN 13641:2002, German and English texts

DIN EN 13697

Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of bactericidal and/or fungicidal activity of chemical desinfectants used in food, industrial, domestic and institutional areas - Test method and requirements without mechanical action (phase 2/step 2); English version of DIN EN 13697

DIN EN 13718-1

Air, water and difficult-terrain ambulances - Part 1: Medical device interface requirements for the continuity of patient care

DIN EN 13718-2

Air, water and difficult-terrain ambulances - Part 2: Operational and technical requirements for the continuity of patient care

DIN EN 13726-1

Test methods for primary wound dressings - Part 1: Aspects of absorbency

DIN EN 13726-2

Test methods for primary wound dressings - Part 2: Moisture vapour transmission rate of permeable film dressings

DIN EN 13726-3

Non-active medical devices - Test methods for primary wound dressings - Part 3: Waterproofness

DIN EN 13726-4

Non-active medical devices - Test methods for primary wound dressings - Part 4: Conformability

DIN EN 13726-6

Non-active medical devices - Test methods for primary wound dressings - Part 6: Odour control

DIN EN 13727

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)

DIN EN 13783

Foodstuffs - Detection of irradiated food using Direct Epifluorescent Filter Technique/Aerobic Plate Count (DEFT/APC) - Screening method

DIN EN 13795-1

Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Part 1: General requirements for manufacturers, processors and products

DIN EN 13795-2

Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods

DIN EN 13795-3

Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 3: Performance requirements and performance levels

DIN EN 13798

Hydrometry - Specification for a reference raingauge pit

DIN EN 13826

Peak expiratory flow meters

DIN EN 13867

Concentrates for haemodialysis and related therapies

DIN EN 13868

Catheters - Test methods for kinking of single lumen catheters and medical tubing

DIN EN 13975

Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects; German version EN 13975:2003, German and English texts

DIN EN 13976-1

Rescue systems - Transportation of incubators - Part 1: Interface conditions

DIN EN 13976-2

Rescue systems - Transportation of incubators - Part 2: System requirements

DIN EN 14065

Textiles - Laundry processed textiles - Biocontamination control system

DIN EN 14079

Non-active medical devices - Performance requirements and test methods for absorbent cotton gauze and absorbent cotton and viscose gauze

DIN EN 14119

Testing of textiles - Evaluation of the action of microfungi

DIN EN 14131

Foodstuffs - Determination of folate by microbiological assay

DIN EN 14136

Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures

DIN EN 14139

Ophthalmic optics - Specifications for ready-to-wear spectacles

DIN EN 14139 Berichtigung 1

Ophthalmic optics - Specifications for ready-to-wear spectacles; Corrigendum 1 to English version of DIN EN 14139:2003-03

DIN EN 14180

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing

DIN EN 14204

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)

DIN EN 1422

Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods

DIN EN 14254

In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans

DIN EN 14299

Non active surgical implants - Particular requirements for cardiac and vascular implants - Specific requirements for arterial stents

DIN EN 14347

Chemical disinfectants and antiseptics - Basic sporicidal activity - Test method and requirements (phase 1)

DIN EN 14348

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)

DIN EN 14375

Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing

DIN EN 14391

Packaging - Collapsible aluminium tubes - Tactile warnings of danger

DIN EN 14476

Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1)

DIN EN 14476

Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1)

DIN EN 14486

Water quality - Detection of human enteroviruses by monolayer plaque assay

DIN EN 14561

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)

DIN EN 14562

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)

DIN EN 14569

Foodstuffs - Microbiological screening for irradiated food using LAL/GNB procedures

DIN EN 14675

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)

DIN EN 14683

Surgical masks - Requirements and test methods

DIN EN 14820

Single-use containers for human venous blood specimen collection

DIN EN 14885

Chemical disinfectants and antiseptics - Application of European Standards for chemical disinfectants and antiseptics

DIN EN 14931

Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety requirements and testing

DIN EN 1499

Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)

DIN EN 1500

Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)

DIN EN 1615

Enteral feeding catheters and enteral giving sets for single use and their connectors - Design and testing; English version of DIN EN 1615

DIN EN 1616

Sterile urethral catheters for single use (includes Amendment A1:1999)

DIN EN 1617

Sterile drainage catheters and accessory devices for single use; German version EN 1617:1997

DIN EN 1618

Catheters other than intravascular catheters - Test methods for common properties; German version EN 1618:1997

DIN EN 1619

Large-scale process and production in biotechnology - General requirements for management and organization for strain preservation procedures

DIN EN 1620

Large-scale process and production in biotechnology - Design of plant buildings according to the degree of hazard

DIN EN 1639

Dentistry - Medical devices for dentistry - Instruments

DIN EN 1640

Dentistry - Medical devices for dentistry - Equipment

DIN EN 1641

Dentistry - Medical devices for dentistry - Materials

DIN EN 1642

Dentistry - Medical devices for dentistry - Dental implants

DIN EN 1644-1

Test methods for nonwoven compresses for medical use - Part 1: Nonwovens used in the manufacture of compresses; German version EN 1644-1:1997

DIN EN 1644-2

Test methods for nonwoven compresses for medical use - Part 2: Finished compresses; English version of DIN EN 1644-2

DIN EN 1650

Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas - Test method and requirements (phase 2/step 1)