YY/T 0606.10-2008
Active
Industry standards-Medicine
YY/T 0606.10-2008 Tissue engineered medical product—Part 10:In vivo assessment of implantable devices intended to repair or regenerate articular cartilage
YY/T 0606.10-2008 Tissue engineered medical product—Part 10:In vivo assessment of implantable devices intended to repair or regenerate articular cartilage
Basic Information
Standard Code:
YY/T 0606.10-2008
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Extracorporeal circulation, artificial organs, and prosthetic devices
ICS Name:
Surgical implants, prostheses, and orthoses
Publish Date:
2008-04-25
Implement Date:
2009-06-01
Pages:
10 pages
Scope
This part of YY/T 0606 specifies the general principles for the in vivo evaluation of implants used to repair or regenerate joint cartilage. The implants described in this part may be composed of natural or synthetic biomaterials (which are biocompatible and biodegradable), or their composites, and may contain cells, drugs, growth factors, synthetic polypeptides, plasmids, or cDNA, among other biologically active factors. This part describes animal models of different species such as rabbits, dogs, pigs, goats, and sheep, and the corresponding experimental procedures, as well as methods for determining and evaluating results such as morphological, histochemical, and biomechanical analyses.
Development Information
Same series standard
Referenced Standards
Related Standards
GB 12264-1990
Replaced
GB 12279-1990
Replaced
GB 12279-1990 Cardiac valve prostheses general technical specification
GB 12417-1990
Replaced
GB 12417-1990 The general technological conditions of surgical metal implant
GB/T 13461-1992
Replaced
GB/T 13461-1992 Synthetic resin blow knee prostheses
GB/T 14191-1993
Replaced
GB/T 14191-1993 Terminology for prosthetics and orthotics
GB 14722-1993
Replaced