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Fiberoptic Dual End Cable

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
Fiberoptic Dual End Cable FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
Alif Fiberoptic Dual End Cable FDA UDI
Model / Reference
7332-60 FDA UDI
Description
Alif Fiberoptic Dual End Cable FDA UDI

Identifiers

Catalog Number
7332-60 FDA UDI
Primary DI / UDI-DI
10840199515995 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic light cable

Fiberoptic Dual End Cable by Koros USA, 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

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI a4441ca2-3afe-4a0c-a3b6-be41e569bf27 37 fields · synced Jun 8, 2026