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Universal Light Guide Adapter

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Universal Light Guide Adapter FDA UDI
Generic Name
Endoscopic light source adaptor FDA UDI
Device Name
MAJ-1200 CLV-S40 UNIVERSAL LIG HT GUIDE FDA UDI
Model / Reference
OLYMPUS MAJ-1200 FDA UDI
Description
MAJ-1200 CLV-S40 UNIVERSAL LIG HT GUIDE FDA UDI

Identifiers

Primary DI / UDI-DI
04953170155017 FDA UDI
FDA Product Code
FDS FDA UDI
GMDN Term
Endoscopic light source adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic light source adaptor

Universal Light Guide Adapter by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic light source adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 684bfd67-f5f4-478b-9df0-77c8da9bf508 34 fields · synced Jun 1, 2026