Identity
- Trade Name
- 2.0 × 8.0 mm Screw FDA UDI
- Generic Name
- Craniofacial bone screw, non-bioabsorbable FDA UDI
- Device Name
- 2.0 × 8.0 mm Screw FDA UDI
- Model / Reference
- 500094 FDA UDI
- Description
- 2.0 × 8.0 mm Screw FDA UDI
Identifiers
- Primary DI / UDI-DI
- M9575000940 FDA UDI
- FDA Product Code
- MPI FDA UDILZD FDA UDI
- GMDN Term
- Craniofacial bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 872.3950 FDA UDI872.3940 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
Yes
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
2.0 × 8.0 mm Screw by Nexus Cmf, L.L.C. — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- Nexus Cmf, L.L.C.
Sources (1)
- FDA UDI 55bd7013-f462-4ee0-b6dd-fa8656a6947a 34 fields · synced May 30, 2026