← Back to catalogue

MI Product Line

FDA UDI

Class I (US FDA UDI)

by Medical Illumination International, Inc

Identity

Trade Name
MI Product Line FDA UDI
Generic Name
Mobile examination/treatment room light FDA UDI
Device Name
MI-550 Examination Light, Floor Stand FDA UDI
Model / Reference
061323 FDA UDI
Description
MI-550 Examination Light, Floor Stand FDA UDI

Identifiers

Primary DI / UDI-DI
00816835020225 FDA UDI
FDA Product Code
KZF FDA UDI
GMDN Term
Mobile examination/treatment room light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6320 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

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: Mobile examination/treatment room light

MI Product Line by Medical Illumination International, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile examination/treatment room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medical Illumination International, Inc

Sources (1)

  • FDA UDI cac14b13-5cb5-4cec-a510-9c32b2b8626c 33 fields · synced May 30, 2026