Identity
- Trade Name
- ORTHOMED FDA UDI
- Generic Name
- Bone holding forceps FDA UDI
- Device Name
- BISHOP BONE CLAMP 9" ADJUSTABLE FDA UDI
- Model / Reference
- OM 47-0202 FDA UDI
- Description
- BISHOP BONE CLAMP 9" ADJUSTABLE FDA UDI
Identifiers
- Primary DI / UDI-DI
- B8034702020 FDA UDI
- FDA Product Code
- HXD FDA UDI
- GMDN Term
- Bone holding forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone holding forceps
Orthomed by Ortho-Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone holding forceps.
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- CLAMP — KLS-Martin L.P. · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Tecomet — Tecomet,Inc · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Ortho-Med, Inc.
Sources (1)
- FDA UDI f93b472f-aaf4-4428-96ed-509a67cece2c 33 fields · synced May 31, 2026