Identity
- Trade Name
- Adult Arm and Hand Table, No Pad FDA UDI
- Generic Name
- Orthopaedic operating table top FDA UDI
- Device Name
- Carbon fiber construction radiolucent surgical table attachment sized for adult patients. Attached to surgical table side rails via and accessory clamp. FDA UDI
- Model / Reference
- 1-1014-005 FDA UDI
- Description
- Carbon fiber construction radiolucent surgical table attachment sized for adult patients. Attached to surgical table side rails via and accessory clamp. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810105030754 FDA UDI
- FDA Product Code
- BWN FDA UDI
- GMDN Term
- Orthopaedic operating table top FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4950 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic operating table top
Adult Arm and Hand Table, No Pad by Composite Manufacturing, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic operating table top.
- ISI — INSTRUMENT SPECIALISTS, INC. · Class I
- Carter — INSTRUMENT SPECIALISTS, INC. · Class I
- ISI — INSTRUMENT SPECIALISTS, INC. · Class I
- Carter — INSTRUMENT SPECIALISTS, INC. · Class I
- C-Thru — INSTRUMENT SPECIALISTS, INC. · Class I
- Carter — INSTRUMENT SPECIALISTS, INC. · Class I
- C-Thru — INSTRUMENT SPECIALISTS, INC. · Class I
- Arthrex® — Arthrex, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Composite Manufacturing, Inc.
Sources (1)
- FDA UDI 62162205-987e-479b-a132-1acb7f68ad3c 33 fields · synced Jun 8, 2026