EN ISO 10993-17

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

2009-04-00

Có hiệu lực

DIN EN ISO 10993-17 (2009-08), IDT * BS EN ISO 10993-17 (2009-06-30), IDT * NF S99-501-17 (2009-08-01), IDT * ISO 10993-17 (2002-12), IDT * SN EN ISO 10993-17 (2009-08), IDT * OENORM EN ISO 10993-17 (2009-09-15), IDT * PN-EN ISO 10993-17 (2009-09-17), IDT * SS-EN ISO 10993-17 (2009-05-08), IDT * UNE-EN ISO 10993-17 (2009-09-09), IDT * TS EN ISO 10993-17 (2013-02-21), IDT * UNI EN ISO 10993-17:2009 (2009-07-02), IDT * STN EN ISO 10993-17 (2009-08-01), IDT * CSN EN ISO 10993-17 (2009-11-01), IDT * DS/EN ISO 10993-17 (2009-07-02), IDT * NEN-EN-ISO 10993-17:2009 en (2009-05-01), IDT * SFS-EN ISO 10993-17:en (2009-10-30), IDT

ISO 10993-1 (2003-08) * 90/385/EWG (1990-06-20) * 93/42/EWG (1993-06-14)

EN ISO 10993-17 (2002-12) * prEN ISO 10993-17 (2008-12)

EN ISO 10993-17 (2009-04) * EN ISO 10993-17 (2002-12) * prEN ISO 10993-17 (2008-12) * prEN ISO 10993-17 (2002-05) * prEN ISO 10993-17 (1999-08)

Allowable * Alloys * Bioassay * Biological analysis and testing * Biological tests * Decomposition * Decomposition products * Definitions * Degradability * Degradation * Deterioration * Determination * Establishment * Evaluations * Health hazards * Identification * Limits (mathematics) * Medical devices * Medical equipment * Medical products * Metals * Methods * Quantification * Residues * Risk analysis * Soluble * Testing * Toxicological testing

11.100.20. Đánh giá sinh học các thiết bị y tế, Vi sinh y khoa, xem 07.100.10

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