Identity
- Trade Name
- AtoN Keywest Headlight without Fiber Optic Cable FDA UDI
- Generic Name
- Endoscopic light source unit, line-powered FDA UDI
- Device Name
- Light, Surgical, Endoscopic, Accessory FDA UDI
- Model / Reference
- P003267 FDA UDI
- Description
- Light, Surgical, Endoscopic, Accessory FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851610007091 FDA UDI
- FDA Product Code
- FSW FDA UDI
- GMDN Term
- Endoscopic light source unit, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endoscopic light source unit, line-powered
AtoN Keywest Headlight without Fiber Optic Cable by Long Island Tech — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- FUJIFILM — FUJIFILM Corporation · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Long Island Tech
Sources (1)
- FDA UDI dea39f3b-6e73-407d-9b23-a81889425c22 33 fields · synced May 30, 2026