Drill guide 5913
by Zimmer, Inc.
Ref 5913
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 | Number889024YEL5 | Date20 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889024301290 | Date16 Nov 2018 | 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- Withdrawn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
- Drill guide
- Generic Name
- Joint prosthesis implantation kit, reusable
- Model / Ref / Catalog
- 5913
- Primary DI / UDI-DI
- 00889024301290
- Basic UDI-DI
- 889024YEL5
- FDA Product Code
- FZX
- EMDN Code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN Term
- Joint prosthesis implantation kit, reusable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Market of Registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Zimmer, Inc.
Properties
Other properties (18)
- 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