Wire bending forceps 100.11.155
by Zimmer, Inc. EUDAMEDGUDID
Active
Ref 100.11.155
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number889024NEK4 | Date19 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889024297920 | Date30 Jun 2020 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- Wire bending forceps
- Generic Name
- General internal orthopaedic fixation system implantation kit
- Model / Ref / Catalog
- 100.11.155
- Primary DI / UDI-DI
- 00889024297920
- Basic UDI-DI
- 889024NEK4
- Direct Marketing DI
- 00889024297920
- FDA Product Code
- HTD
- EMDN Code
- L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
- GMDN Term
- General internal orthopaedic fixation system implantation kit
- 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