BS EN ISO 10993-16:2010

Заменен

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables — 22 стр.

Ссылочные документы

Действует

Medical devices -- Application of risk management to medical devices — 90 стр.

Действует

Biological evaluation of medical devices -- Part 18: Chemical characterization of materials — 24 стр.

Действует

Biological evaluation of medical devices. Part 17. Establishment of allowable limits for leachable substances — 31 стр.

Действует

Biological evaluation of medical devices -- Part 12: Sample preparation and reference materials — 28 стр.

Действует

Biological evaluation of medical devices -- Part 2: Animal welfare requirements — 20 стр.

Заменен

Biological evaluation of medical devices -- Part 11: Tests for systemic toxicity — 34 стр.

Действует

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables — 22 стр.

Заменен

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables — 20 стр.

Заменен

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables — 20 стр.

Действует

Cardiovascular implants and extracorporeal systems. Vascular prostheses. Tubular vascular grafts and vascular patches — 68 стр.

Действует

Biological evaluation of medical devices. Tests for local effects after implantation — 44 стр.

Действует

Biological evaluation of medical devices. Toxicokinetic study design for degradation products and leachables — 22 стр.