Identity
- Trade Name
- primaLOK FF FDA UDI
- Generic Name
- Cannulated surgical drill bit, reusable FDA UDI
- Device Name
- 3mm Cannulated Power Drill FDA UDI
- Model / Reference
- 800-1221 FDA UDI
- Description
- 3mm Cannulated Power Drill FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00813210022157 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Cannulated surgical drill bit, reusable 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
Category: Cannulated surgical drill bit, reusable
primaLOK FF by Wenzel Spine — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cannulated surgical drill bit, reusable.
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- EBA2 — Citieffe · Class II
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
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- BIXCUT — Stryker Corp. · Class I
- FREE GLIDING SCFE SCREW SYSTEM — Orthopediatrics Canada ULC · 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
- Wenzel Spine
Sources (1)
- FDA UDI 6b655f98-ba8a-4c62-b285-939382b4e5b6 34 fields · synced May 30, 2026