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Midmark 153600-001

by Midmark Corporation

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841709111846 UDI-DIDate28 Sep 2026ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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
Dental delivery system instrument unit, electric
Model / Ref / Catalog
153600-001
Primary DI / UDI-DI
00841709111846
510(k) Number
FDA Product Code
EIA
GMDN Term
Dental delivery system instrument unit, electric
Device Class
Class I
Regulation Number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K003090)

Show all (12)

Other devices from Midmark Corporation

See all devices from Midmark Corporation →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No