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Comeg Medical

FDA UDI

Class II (US FDA UDI)

by Sopro

Identity

Trade Name
COMEG MEDICAL FDA UDI
Generic Name
Endoscopic light source unit, line-powered FDA UDI
Device Name
Xenon light source 180 Watts, US Power Cord - Olympus adapter FDA UDI
Model / Reference
S218 SOPRO US OLYMPUS FDA UDI
Description
Xenon light source 180 Watts, US Power Cord - Olympus adapter FDA UDI

Identifiers

Catalog Number
S_218_0011 FDA UDI
Primary DI / UDI-DI
M430S21800111 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic light source unit, line-powered 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic light source unit, line-powered

Comeg Medical by Sopro — 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

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Manufacturer

Manufacturer
Sopro

Sources (1)

  • FDA UDI 964d8fe2-6e3a-4182-b929-17497f5d4324 35 fields · synced Jun 8, 2026