Identity
- Trade Name
- MD Vue Lateral Access FDA UDI
- Generic Name
- Neurosurgical retraction system, spinal FDA UDI
- Device Name
- Bifurcated Illuminator FDA UDI
- Model / Reference
- 54-LC-5200 FDA UDI
- Description
- Bifurcated Illuminator FDA UDI
Identifiers
- Catalog Number
- 54-LC-5200 FDA UDI
- Primary DI / UDI-DI
- 00840019919593 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Neurosurgical retraction system, spinal 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MD Vue Lateral Access by Precision Spine, 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
- Precision Spine, Inc.
Sources (1)
- FDA UDI 57248379-23f3-45b9-a407-89b18318f246 35 fields · synced Jun 1, 2026