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Precision Spine TLIF Bifurcated Surgical Illuminator
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Precision Spine TLIF Bifurcated Surgical Illuminator FDA UDI
- Generic Name
- Open surgical site internal light FDA UDI
- Model / Reference
- 73-LC-5200 FDA UDI
Identifiers
- Catalog Number
- 012628 FDA UDI
- Primary DI / UDI-DI
- 00812432022662 FDA UDI
- FDA Product Code
- FDG FDA UDI
- GMDN Term
- Open surgical site internal light FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4530 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Precision Spine TLIF Bifurcated Surgical Illuminator by Lumitex, Inc. — 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
- Lumitex, Inc.
Sources (1)
- FDA UDI d1a4e533-ec2b-4a8a-be9c-5e73ec2e484d 34 fields · synced May 29, 2026