DIN EN ISO 18113-4:2013-01
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 4: IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING (ISO 18113-4:2009) |
I.S. EN 1041:2008+A1:2013
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INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
06/30123163 DC : 0
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BS EN 1041 - INFORMATION SUPPLIED BY THE MANUFACTURER WITH MEDICAL DEVICES |
BS ISO 17593:2007
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Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy |
BS EN ISO 18113-4:2011
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In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) In vitro diagnostic reagents for self-testing |
UNI EN ISO 18113-4 : 2012
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 4: IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
UNI CEI EN 980 : 2009
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SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
BS EN 13641:2002
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Elimination or reduction of risk of infection related to in vitro diagnostic reagents |
EN 12376:1999
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In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology |
ISO 17593:2007
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Clinical laboratory testing and in vitro medical devices Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy |
I.S. EN 592:2002
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INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING |
06/30146522 DC : 0
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BS ISO 18113-4 - CLINICAL LABORATORY TESTING AND IN VITRO DIAGNOSTIC MEDICAL SYSTEMS - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 4: IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
UNE-EN ISO 18113-4:2012
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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) |
00/563139 DC : DRAFT JUL 2000
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BS ISO 19001 - IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR STAINING IN BIOLOGY |
CSA Z22870 : 2007 : R2013
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POINT-OF-CARE TESTING (POCT) - REQUIREMENTS FOR QUALITY AND COMPETENCE |
CSA Z22870:2007
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POINT-OF-CARE TESTING (POCT) - REQUIREMENTS FOR QUALITY AND COMPETENCE |
CEI UNI EN 1041 : 2014
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INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
UNE-EN ISO 18113-1:2012
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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) |
ISO/TR 18112:2006
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Clinical laboratory testing and in vitro diagnostic test systems In vitro diagnostic medical devices for professional use Summary of regulatory requirements for information supplied by the manufacturer |
DIN EN 1041:2013-12
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Information supplied by the manufacturer of medical devices (includes Amendment A1:2013) |
EN 1041:2008+A1:2013
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Information supplied by the manufacturer of medical devices |
DD ENV 13607:2000
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Health informatics. Messages for the exchange of information on medicine prescriptions |
04/30090846 DC : DRAFT JUL 2004
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BS ISO 22870 - POINT-OF-CARE TESTING (POCT) - REQUIREMENTS FOR QUALITY AND COMPETENCE |
I.S. ENV 13607:2000
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HEALTH INFORMATICS - MESSAGES FOR THE EXCHANGE OF INFORMATION ON MEDICINE PRESCRIPTIONS |
ENV 13607:2000
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HEALTH INFORMATICS - MESSAGES FOR THE EXCHANGE OF INFORMATION ON MEDICINE PRESCRIPTIONS |
I.S. EN 12376:1999
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR STAINING IN BIOLOGY |
00/560160 DC : DRAFT JAN 2000
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BS ISO 15197 DETERMINATION OF PERFORMANCE CRITERIA FOR IN VITRO BLOOD GLUCOSE MONITORING SYSTEMS FOR MANAGEMENT OF HUMAN DIABETES MELLITUS |
02/563809 DC : DRAFT SEP 2002
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BS EN 980 - GRAPHICAL SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
09/30176675 DC : 0
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BS EN ISO 15223-1 - MEDICAL DEVICES - SYMBOLS TO BE USED WITH MEDICAL DEVICE LABELS, LABELLING AND INFORMATION TO BE SUPPLIED - PART 1: GENERAL REQUIREMENTS |
UNI CEI EN 1041 : 2013
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INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
I.S. EN ISO 18113-1:2011
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS (ISO 18113-1:2009) |
06/30146511 DC : 0
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BS ISO 18113-1 - CLINICAL LABORATORY TESTING AND IN VITRO DIAGNOSTIC MEDICAL SYSTEMS - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS |
DD ENV 12610:1998
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Medical informatics. Medical product identification |
I.S. EN ISO 18113-4:2011
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 4: IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING (ISO 18113-4:2009) |
BS EN 13612:2002
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Performance evaluation of in vitro diagnostic medical devices |
BS EN 13532:2002
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General requirements for in vitro diagnostic medical devices for self-testing |
UNE-EN 1041:2009
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Information supplied by the manufacturer of medical devices |
ISO 18113-4:2009
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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing |
BS EN 1041 : 2008
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INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES |
ISO 18113-1:2009
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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
BS EN 12376:1999
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In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology |
EN 592 : 2002
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INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING |
EN 13641:2002
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Elimination or reduction of risk of infection related to in vitro diagnostic reagents |
EN 980:2008
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Symbols for use in the labelling of medical devices |
EN ISO 18113-1:2011
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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) |
EN 13612:2002/AC:2002
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PERFORMANCE EVALUATION OF IN VITRO DIAGNOSTIC MEDICAL DEVICES |
I.S. EN 980:2008
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SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
DIN EN ISO 18113-1:2013-01
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS (ISO 18113-1:2009) |
BS EN ISO 18113-1:2011
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In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements |
06/30122245 DC : 0
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EN 980 - SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
UNI EN ISO 18113-1 : 2012
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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS |
BS EN 592:2002
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Instructions for use for in vitro diagnostic instruments for self-testing |
BS EN 980:2008
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Symbols for use in the labelling of medical devices |
EN 13532:2002
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General requirements for in vitro diagnostic medical devices for self-testing |
DIN EN 980:2003-08
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SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |