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Medicom Pro-Matrix 30030

by AMD Medicom Inc

Listed FDA GUDID listing, not in commercial distribution

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 Number10686864054853 UDI-DI Date18 Jan 2019ListedStatusListed GUDID: not 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  • Withdrawn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
Medicom Pro-Matrix
Generic name
Dental matrix band, single-use
Model / Ref / Catalog
30030
Primary DI / UDI-DI
10686864054853
FDA product code
DZN
GMDN term
Dental matrix band, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
Not in Commercial Distribution

Other devices from AMD Medicom Inc

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No