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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
Midmark LED retrofit kit to bring the performance and efficiency of the Midmark LED operatory light to the Universal Mounted Midmark Operatory Lights. FDA UDI
Model / Reference
002-1536-00 FDA UDI
Description
Midmark LED retrofit kit to bring the performance and efficiency of the Midmark LED operatory light to the Universal Mounted Midmark Operatory Lights. FDA UDI

Identifiers

Catalog Number
002-1536-00 FDA UDI
Primary DI / UDI-DI
00841709109546 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 8d2e477f-3e31-4d59-8e5c-ee2c9e596b05 36 fields · synced Jun 8, 2026