Identity
- Trade Name
- K-WIRE FDA UDI
- Generic Name
- Orthopaedic bone wire FDA UDI
- Model / Reference
- 110018527 FDA UDI
Identifiers
- Catalog Number
- 110018527 FDA UDI
- Primary DI / UDI-DI
- 00887868137907 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Orthopaedic bone wire FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic bone wire
K-Wire by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- mahe medical GmbH — mahe medical gmbh · Class II
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Cleared under the same submission
K142658 also covers:
- 0.9MM K-WIRE DEPTH GAUGE — Biomet Orthopedics, Inc.
- Cannulated Drill Bit AO — Biomet Orthopedics, Inc.
- HEAD RELIEF DRILL AO — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
- HEADLESS COMPRESSION SCREW — Biomet Orthopedics, Inc.
K190035 also covers:
- 0.9MM K-WIRE DEPTH GAUGE — Biomet Orthopedics, Inc.
- CANNULATED DRILL BIT AO — Biomet Orthopedics, Inc.
- CANNULATED DRILL BIT AO — Biomet Orthopedics, Inc.
- Cannulated Drill Bit AO — Biomet Orthopedics, Inc.
- Cannulated Drill Bit AO — Biomet Orthopedics, Inc.
- HEAD RELIEF DRILL BIT AO — Biomet Orthopedics, Inc.
- HEAD RELIEF DRILL BIT AO — Biomet Orthopedics, Inc.
- Head Relief Drill Bit AO — Biomet Orthopedics, Inc.
- Head Relief Drill Bit AO — Biomet Orthopedics, Inc.
- K-WIRE — Biomet Orthopedics, Inc.
- K-WIRE — Biomet Orthopedics, Inc.
- K-Wire — Biomet Orthopedics, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI bb6535a6-3e02-40f6-9522-83899c586a9a 36 fields · synced Jun 8, 2026