← Back to catalogue

AtoN Keywest Headlight without Fiber Optic Cable

FDA UDI

Class II (US FDA UDI)

by Long Island Tech

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

Similar devices

Also classified as Endoscopic light source unit, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Long Island Tech

Sources (1)

  • FDA UDI dea39f3b-6e73-407d-9b23-a81889425c22 33 fields · synced May 30, 2026