LinkBio Instrument 87-1118
LinkBio Instrument 87-1118 is a Class I device made by LinkBio Corp., listed in FDA GUDID since 4 Nov 2020 (UDI-DI 00810022401866), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810022401866 | Date4 Nov 2020 | StatusListed |
Official records
- AccessGUDID record 00810022401866
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LinkBio Instrument
- Generic name
- Knee femur prosthesis trial, reusable
- Model / Ref / Catalog
- 87-1118
- Primary DI / UDI-DI
- 00810022401866
- FDA product code
- HWT
- GMDN term
- Knee femur prosthesis trial, reusable
- Device class
- Class I
- Regulation number
- 888.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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