Gryphon 210826
Ref 210826Model General Orthopedic Use Aiming and Guiding Instruments
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0886705a00120K2 | Date21 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10886705024131 | Date1 Sep 2015 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Gryphon
- Generic Name
- Orthopaedic guidewire, reusable
- Model / Ref / Catalog
- 210826, General Orthopedic Use Aiming and Guiding Instruments
- Primary DI / UDI-DI
- 10886705024131
- Basic UDI-DI
- 0886705a00120K2
- Direct Marketing DI
- 10886705024131
- FDA Product Code
- LXH
- EMDN Code
- Z12139099 Various orthopaedic and traumatology instruments - other
- GMDN Term
- Orthopaedic guidewire, reusable
- Device Class
- Class I
- Regulation Number
- 888.4540
- Market of Registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from DePuy Mitek, Inc.
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No