Identity
- Trade Name
- Lateral Retractor FDA UDI
- Generic Name
- Light source adaptor FDA UDI
- Device Name
- 3.5mm Bifurcated Cable FDA UDI
- Model / Reference
- 95-6775 FDA UDI
- Description
- 3.5mm Bifurcated Cable FDA UDI
Identifiers
- Catalog Number
- 95-6775 FDA UDI
- Primary DI / UDI-DI
- 10889981098858 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Light source adaptor 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
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
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: Light source adaptor
Lateral Retractor by SeaSpine Orthopedics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Light source adaptor.
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- Aspen® Flexible Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
- Innomed, Inc. — Innomed, Inc. · Class II
- Aspen® Rigid Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
- SPOTLIGHT — Depuy Spine, Inc. · 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
- SeaSpine Orthopedics Corporation
Sources (1)
- FDA UDI bb3c4c2e-bd8c-4d50-9589-56e80d7f860d 36 fields · synced Jun 8, 2026