The European legislation on medical devices

Studies in Health Technology and Informatics

Volumn 28, Issue , 1996, Pages 5-12

  Anselmann, Norbert ^a  

^a EUROPEAN COMMISSION   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

EUROPEAN LEGISLATION; HEALTH AND SAFETY; MEDICAL DEVICES;

LAWS AND LEGISLATION;

APPARATUS, EQUIPMENT AND SUPPLIES; ARTICLE; EQUIPMENT; EUROPEAN UNION; MEDICOLEGAL ASPECT; STANDARD;

EQUIPMENT AND SUPPLIES; EQUIPMENT SAFETY; EUROPEAN UNION; LEGISLATION, MEDICAL;

EID: 0030330111     PISSN: 09269630     EISSN: 18798365     Source Type: Book Series    
DOI: 10.3233/978-1-60750-872-4-5     Document Type: Article

References (8)

1. Official Journal Nr. L 189, 20.07.1990
2. Official Journal Nr. L 169, 12.07.1993
3. Official Journal Nr. C 172, 07.07.1995
4. Official Journal Nr. C 136/1, 04.06.1985
5. A global concept on certification and testing, COM(89) 209 of 24.7.1989; decision 93/465/EEC of the Council relating to the certification modules to be used in directives of technical harmonisation and on the rules for the affixing of the CE marking, OJ no. L220, 30.08.1993, p. 23
6. Official Journal Nr. C 277/6, 04.10.1994 + C 204/22, 09.08.1995 + C 304/14, 18.11.1995
7. Decision 93/465/EEC, Official Journal Nr. L 220/23, 30.08.1993
8. Official Journal Nr. C 280/1, 25.10.1995