ASTM F2451-05

Заменен

Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage — 9 стр.

Описание Ссылки Версии

Ссылочные документы

ASTM F2150-07

Заменен

Standard Guide for Characterization and Testing of Biomaterial Scaffolds Used in Tissue-Engineered Medical Products — 10 стр.

ASTM F1983-99(2008)

Заменен

Standard Practice for Assessment of Compatibility of Absorbable/Resorbable Biomaterials for Implant Applications — 5 стр.

ASTM F981-04(2010)

Заменен

Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone — 5 стр.

ASTM F895-84(2006)

Заменен

Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity — 5 стр.

ASTM F565-04(2009)e1

Заменен

Standard Practice for Care and Handling of Orthopedic Implants and Instruments — 2 стр.

ASTM F561-05a

Заменен

Standard Practice for Retrieval and Analysis of Medical Devices, and Associated Tissues and Fluids — 16 стр.

ASTM F2451-05(2010)

Отменен

Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage (Withdrawn 2019) — 9 стр.

На этот документ ссылаются

DIN ISO 13022:2014-06

Действует

Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012) — 62 стр.

ASTM F2721-08

Заменен

Standard Guide for Pre-clinical in vivo Evaluation in Critical Size Segmental Bone Defects — 13 стр.

ASTM F2451-05(2010)

Отменен

Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage (Withdrawn 2019) — 9 стр.