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Fiberoptics Technology INC

FDA UDI

Class I (US FDA UDI)

by Fiberoptics Technology, Inc.

Identity

Trade Name
Fiberoptics Technology INC FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
Fiber Optic Medical Light Guide 3.5mm FDA UDI
Model / Reference
FTIMG 3.5mm FDA UDI
Description
Fiber Optic Medical Light Guide 3.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
00862658000333 FDA UDI
FDA Product Code
EQH FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4350 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

No

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

Yes

FDA UDI

Category: Fibreoptic light cable

Fiberoptics Technology INC by Fiberoptics Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be2cc40d-97fb-4290-8038-2148f66f4103 33 fields · synced May 30, 2026