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Xenon 300 Plus

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
XENON 300 PLUS FDA UDI
Generic Name
Endoscopic light source unit, line-powered FDA UDI
Device Name
Cold Light Fountain XENON 300 SCB FDA UDI
Model / Reference
20133120-1 FDA UDI
Description
Cold Light Fountain XENON 300 SCB FDA UDI

Identifiers

Primary DI / UDI-DI
04048551062890 FDA UDI
FDA Product Code
GCT 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

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

Xenon 300 Plus by Karl Storz GmbH & Co. KG — 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

Sources (1)

  • FDA UDI e3374852-3a72-4aaf-964a-e781faa02861 33 fields · synced May 29, 2026