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Midmark

FDA UDI

Class I (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark FDA UDI
Generic Name
LED dental light, line-powered FDA UDI
Device Name
Trolley and track assembly used on 96 inch Midmark Dental LED Lights and Monitors. FDA UDI
Model / Reference
029-7245-00 FDA UDI
Description
Trolley and track assembly used on 96 inch Midmark Dental LED Lights and Monitors. FDA UDI

Identifiers

Catalog Number
1531018-010 / 153964-010 FDA UDI
Primary DI / UDI-DI
00841709107009 FDA UDI
FDA Product Code
EAZ FDA UDI
GMDN Term
LED dental light, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4630 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

Yes

FDA UDI

Category: LED dental light, line-powered

Midmark by Midmark Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as LED dental light, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI af877d3a-1894-49ba-89df-0d614e9451d6 36 fields · synced Jun 8, 2026