Identity
- Trade Name
- MAXFRAME FDA UDI
- Generic Name
- Wire holding/twisting forceps FDA UDI
- Device Name
- WIRE TENSIONER FDA UDI
- Model / Reference
- 03.312.001 FDA UDI
- Description
- WIRE TENSIONER FDA UDI
Identifiers
- Catalog Number
- 03312001 FDA UDI
- Primary DI / UDI-DI
- 10886982261106 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Wire holding/twisting forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Wire holding/twisting forceps
Maxframe by Synthes — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Synthes
Sources (1)
- FDA UDI c02d07f5-7884-4b5c-8fef-79c4df0ed8b2 35 fields · synced May 30, 2026