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Midmark

FDA UDI

Class I (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark FDA UDI
Generic Name
Reflective dental room light FDA UDI
Device Name
Trolley and track assembly used on 128 inch Midmark Dental Halogen Lights and Monitors. FDA UDI
Model / Reference
029-7244-08 FDA UDI
Description
Trolley and track assembly used on 128 inch Midmark Dental Halogen Lights and Monitors. FDA UDI

Identifiers

Catalog Number
1531017-008 / 153963-008 FDA UDI
Primary DI / UDI-DI
00841709106996 FDA UDI
FDA Product Code
EAZ FDA UDI
GMDN Term
Reflective dental room light 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: Reflective dental room light

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

Similar devices

Also classified as Reflective dental room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI f8c190aa-8754-45a8-9c81-e3d1200613f6 36 fields · synced Jun 8, 2026