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Midmark 1531018-013

by Midmark Corporation

Midmark 1531018-013 is a Class I device made by Midmark Corporation, listed in FDA GUDID since 9 Jan 2019 (UDI-DI 00841709111761), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841709111761 UDI-DI Date9 Jan 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Midmark
Generic name
LED dental light, line-powered
Model / Ref / Catalog
1531018-013
Primary DI / UDI-DI
00841709111761
FDA product code
EAZ
GMDN term
LED dental light, line-powered
Device class
Class I
Regulation number
872.4630
GUDID distribution status
In Commercial Distribution

Related devices

Category: LED dental light, line-powered

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Other devices filed under LED dental light, line-powered.

Other devices from Midmark Corporation

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)