Identity
- Trade Name
- MatrixMANDIBLE FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- MATRIXMANDIBLE/RIB SCREWDRIVER BLADE/SELF-RETAINING 52MM/QC FDA UDI
- Model / Reference
- SD314.007 FDA UDI
- Description
- MATRIXMANDIBLE/RIB SCREWDRIVER BLADE/SELF-RETAINING 52MM/QC FDA UDI
Identifiers
- Catalog Number
- SD314007 FDA UDI
- Primary DI / UDI-DI
- 10887587002286 FDA UDI
- FDA Product Code
- HXX FDA UDI
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not 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
MatrixMANDIBLE by Synthes (u.s.a.) Lp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 (u.s.a.) Lp
Sources (1)
- FDA UDI 28d238dd-7e18-4781-a75e-7584400562ba 36 fields · synced May 30, 2026