
2007/47/EC : 2007 COR 1 2015
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 5 SEPTEMBER 2007 AMENDING COUNCIL DIRECTIVE 1990/385/EEC ON THE APPROXIMATION OF THE LAWS OF THE MEMBER STATES RELATING TO ACTIVE IMPLANTABLE MEDICAL DEVICES, COUNCIL DIRECTIVE 1993/42/EEC CONCERNING MEDICAL DEVICES AND DIRECTIVE 1998/8/EC CONCERNING THE PLACING OF BIOCIDAL PRODUCTS ON THE MARKET(TEXT WITH EEA RELEVANCE)
Superseded date
05-04-2017
Superseded by
Published date
12-01-2013
Publisher
DevelopmentNote |
COR 1 is only available in Bulgarian, Spanish, Czech, French, Croatian, Latvian, Lithuanian, Polish and Slovak language. (04/2017) Superseded by 2017/745/EU, but remains valid until 25/05/2020. (09/2017)
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DocumentType |
Miscellaneous Product
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PublisherName |
European Union
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Status |
Superseded
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SupersededBy |
08/30184612 DC : DRAFT SEP 2008 | BS EN 1641 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
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15/30321267 DC : DRAFT FEB 2015 | BS EN 50527-1 - PROCEDURE FOR THE ASSESSMENT OF THE EXPOSURE TO ELECTROMAGNETIC FIELDS OF WORKERS BEARING ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL |
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BS PAS 84(2008) : 2008 | REGENERATIVE MEDICINE - GLOSSARY |
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PREN 50527-1 : DRAFT 2015 | PROCEDURE FOR THE ASSESSMENT OF THE EXPOSURE TO ELECTROMAGNETIC FIELDS OF WORKERS BEARING ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL |
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08/30184602 DC : DRAFT SEP 2008 | BS EN 1639 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
ISO 11615:2017 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information |
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08/30184615 DC : DRAFT SEP 2008 | BS EN 1642 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - DENTAL IMPLANTS |
BS EN 50527-1:2016 | Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices General |
UNE-EN ISO 11615:2013 | Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information (ISO 11615:2012) |
IEC TR 60601-4-1:2017 | Medical electrical equipment - Part 4-1: Guidance and interpretation - Medical electrical equipment and medical electrical systems employing a degree of autonomy |
CEN/TR 16953:2017 | Medical gloves for single use - Guidance for selection |
EN ISO 11615:2017 | Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information (ISO 11615:2017) |
EN ISO 11616:2017 | Health informatics - Identification of medicinal products - Data elements and structures for the Unique Identification and Exchange of regulated Pharmaceutical Product Information (ISO 11616:2017) |
S.R. CEN/TR 16953:2017 | MEDICAL GLOVES FOR SINGLE USE - GUIDANCE FOR SELECTION |
13/30271473 DC : 0 | BS EN 80601-2-58 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY |
15/30282343 DC : 0 | BS ISO 18746 - TRADITIONAL CHINESE MEDICINE - INTRADERMAL ACUPUNCTURE NEEDLES |
PD CEN/TR 12401:2009 | Dentistry. Guidance on the classification of dental devices and accessories |
13/30259011 DC : 0 | BS ISO 17218 - STERILE ACUPUNCTURE NEEDLES FOR SINGLE USE |
ISO 18746:2016 | Traditional Chinese medicine — Sterile intradermal acupuncture needles for single use |
16/30344636 DC : 0 | BS EN ISO 11615 - HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR THE UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED MEDICINAL PRODUCT INFORMATION |
I.S. EN 50527-1:2016 | PROCEDURE FOR THE ASSESSMENT OF THE EXPOSURE TO ELECTROMAGNETIC FIELDS OF WORKERS BEARING ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL |
16/30344632 DC : 0 | BS EN ISO 11616 - HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED PHARMACEUTICAL PRODUCT INFORMATION |
BS EN 14683:2014 | Medical face masks. Requirements and test methods |
ISO 23409:2011 | Male condoms Requirements and test methods for condoms made from synthetic materials |
EN 14683:2014 | Medical face masks - Requirements and test methods |
BS EN ISO 14602:2011 | Non-active surgical implants. Implants for osteosynthesis. Particular requirements |
BS EN 1641:2004 | Dentistry. Medical devices for dentistry. Materials |
EN ISO 14602:2011 | Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010) |
EN 1641:2009 | Dentistry - Medical devices for dentistry - Materials |
EN 1639:2009 | Dentistry - Medical devices for dentistry - Instruments |
EN 1640:2009 | Dentistry - Medical devices for dentistry - Equipment |
UNE-EN 50527-1:2011 | Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 1: General |
ISO 17327-1:2018 | Non-active surgical implants — Implant coating — Part 1: General requirements |
ISO 11616:2017 | Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information |
ISO 17218:2014 | Sterile acupuncture needles for single use |
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