AAMI ISO 11607-1 : 2006 : R2010
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS, AND PACKAGING SYSTEMS |
I.S. EN ISO 11810-2:2009
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LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER-RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT-PROTECTIVE COVERS - PART 2: SECONDARY IGNITION |
17/30351717 DC : 0
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BS EN ISO 11607-1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
AAMI ISO 11607-1 : 2006
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS, AND PACKAGING SYSTEMS |
UNE-EN ISO 11607-1:2017
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Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006, including Amd 1:2014) |
I.S. EN 13795-3:2006
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS AND PERFORMANCE LEVELS |
BS EN ISO 11810-1:2009
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Lasers and laser-related equipment. Test method and classification for the laser resistance of surgical drapes and/or patient protective covers Primary ignition and penetration |
DIN EN 13795-2:2009-12
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 2: TEST METHODS |
ISO 11607-2:2006
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Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes |
PREN 13795-3 : DRAFT 2004
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS |
07/30166924 DC : DRAFT AUG 2007
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BS EN 868-2 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: STERILIZATION WRAP - REQUIREMENTS AND TEST METHODS |
DIN EN ISO 11607-2:2014-11
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES (ISO 11607-2:2006 + AMD 1.:2014) |
UNI EN ISO 11810-2 : 2009
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LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER-RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT-PROTECTIVE COVERS - PART 2: SECONDARY IGNITION |
BS EN ISO 11607-2 : 2006
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
AAMI ISO 11607-2:2006
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING, AND ASSEMBLY PROCESSES |
DIN EN ISO 22610:2015-12 (Draft)
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES, FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - TEST METHOD TO DETERMINE THE RESISTANCE TO WET BACTERIAL PENETRATION |
I.S. EN 14126:2003+AC:2004
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PROTECTIVE CLOTHING - PERFORMANCE REQUIREMENTS AND TESTS METHODS FOR PROTECTIVE CLOTHING AGAINST INFECTIVE AGENTS |
DIN EN ISO 11810-1:2009-07
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LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT PROTECTIVE COVERS - PART 1: PRIMARY IGNITION AND PENETRATION |
DIN EN ISO 11810-2:2009-07
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LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER-RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT-PROTECTIVE COVERS - PART 2: SECONDARY IGNITION |
14/30255135 DC : 0
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BS EN ISO 11607-1:2009/A1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
DIN EN ISO 11607-1:2014-11
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006 + AMD 1.:2014) |
17/30351720 DC : 0
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BS EN ISO 11607-2 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
AAMI ISO 11607-2 : 2006 : R2010
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING, AND ASSEMBLY PROCESSES |
ISO 11607-1:2006
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Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
PREN 868-2 : DRAFT 2015
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: STERILIZATION WRAP - REQUIREMENTS AND TEST METHODS |
BS EN ISO 11607-1:2017
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Packaging for terminally sterilized medical devices Requirements for materials, sterile barrier systems and packaging systems |
DIN EN ISO 22612:2005-05
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Clothing for protection against infectious agents - Test method for resistance to dry microbial penetration (ISO 22612:2005); German version EN ISO 22612:2005 |
BS EN ISO 22610:2006
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Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment. Test method to determine the resistance to wet bacterial penetration |
DIN EN ISO 22610:2006-10
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Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006) |
EN ISO 22610:2006
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Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006) |
UNI EN ISO 22612 : 2005
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CLOTHING FOR PROTECTION AGAINST INFECTIOUS AGENTS - TEST METHOD FOR RESISTANCE TO DRY MICROBIAL PENETRATION |
UNI EN ISO 11810-1 : 2009
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LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT PROTECTIVE COVERS - PART 1: PRIMARY IGNITION AND PENETRATION |
UNI EN 13795-3 : 2009
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS AND PERFORMANCE LEVELS |
UNI EN 13795-2 : 2009
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 2: TEST METHODS |
CSA ISO 11607-1 : 2016
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
15/30325855 DC : 0
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BS EN 868-2 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: STERILIZATION WRAP - REQUIREMENTS AND TEST METHODS |
04/30038440 DC : DRAFT NOV 2004
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BS EN 13795-3 - SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS |
ANSI/AAMI/ISO 11607-1:2006/(R)2015
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS, AND PACKAGING SYSTEMS |
CSA ISO 11607-2 : 2016
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
UNI EN ISO 11607-1 : 2014
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
BS EN ISO 11607-1:2020
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Packaging for terminally sterilized medical devices Requirements for materials, sterile barrier systems and packaging systems |
BS EN 14126:2003
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Protective clothing. Performance requirements and tests methods for protective clothing against infective agents |
ISO 22610:2006
|
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment Test method to determine the resistance to wet bacterial penetration |
BS EN 13795-2 : 2004
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SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 2: TEST METHODS |
ISO 11810-1:2005
|
Lasers and laser-related equipment Test method and classification for the laser resistance of surgical drapes and/or patient protective covers Part 1: Primary ignition and penetration |
ISO 22612:2005
|
Clothing for protection against infectious agents Test method for resistance to dry microbial penetration |
ISO 11810-2:2007
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Lasers and laser-related equipment Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers Part 2: Secondary ignition |
BS EN ISO 11810-2:2009
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Lasers and laser-related equipment. Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers Secondary ignition |
EN ISO 11810-2:2009
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Lasers and laser-related equipment - Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers - Part 2: Secondary ignition (ISO 11810-2:2007) |
EN ISO 22612:2005
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Clothing for protection against infectious agents - Test method for resistance to dry microbial penetration (ISO 22612:2005) |
EN 13795-2:2004+A1:2009
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Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods |
EN 13795-3:2006+A1:2009
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Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 3: Performance requirements and performance levels |
EN 14126:2003/AC:2004
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PROTECTIVE CLOTHING - PERFORMANCE REQUIREMENTS AND TESTS METHODS FOR PROTECTIVE CLOTHING AGAINST INFECTIVE AGENTS |
EN ISO 11810-1:2009
|
Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005) |
I.S. EN ISO 11810-1:2009
|
LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD AND CLASSIFICATION FOR THE LASER RESISTANCE OF SURGICAL DRAPES AND/OR PATIENT PROTECTIVE COVERS - PART 1: PRIMARY IGNITION AND PENETRATION |
04/30101211 DC : DRAFT APR 2004
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ISO 11607-1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
UNE-EN ISO 11607-2:2017
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Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006, including Amd 1:2014) |
14/30255138 DC : 0
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BS EN ISO 11607-2:2006/A1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
I.S. EN ISO 11607-2:2017 & LC:2017
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES (ISO 11607-2:2006, INCLUDING AMD 1:2014) |
04/30101215 DC : DRAFT APR 2004
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ISO 11607-2 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
03/107275 DC : DRAFT MAY 2003
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EN ISO 22612 - CLOTHING FOR PROTECTION AGAINST INFECTIOUS AGENTS - TEST METHOD FOR RESISTANCE AGAINST PENETRATION BY BIOLOGICALLY CONTAMINATED DUST |
I.S. EN ISO 11607-1:2017
|
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006, INCLUDING AMD 1:2014) |
BS EN ISO 11607-1 : 2009
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PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
UNI EN ISO 11607-2 : 2014
|
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
DIN EN 14126:2004-01
|
Protective clothing - Performance requirements and test methods for protective clothing against infective agents |
DIN EN 13795-2 E : 2009
|
SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 2: TEST METHODS |
I.S. EN 13795-2:2005
|
SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 2: TEST METHODS |
BS EN ISO 22612:2005
|
Clothing for protection against infectious agents. Test method for resistance to dry microbial penetration |
BS EN 13795-3 : 2006
|
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 13795-3:2009-12
|
SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS AND PERFORMANCE LEVELS |