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1300XSB Xenon Light Source

FDA UDI

Class II (US FDA UDI)

by Medical Illumination International, Inc

Identity

Trade Name
1300XSB Xenon Light Source FDA UDI
Generic Name
General-purpose light source FDA UDI
Device Name
300 Watt Xenon Light Source, Portable FDA UDI
Model / Reference
03-1300XSB FDA UDI
Description
300 Watt Xenon Light Source, Portable FDA UDI

Identifiers

Primary DI / UDI-DI
00816835024155 FDA UDI
510(k) Number
K022384 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
General-purpose light source FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

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: General-purpose light source

1300XSB Xenon Light Source by Medical Illumination International, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose light source.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6ae3297-0cdb-42c7-80ef-6a703f812a26 34 fields · synced May 30, 2026