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Protemp™ Plus 46968

by 3M Deutschland GmbH

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 Number04035077004848 UDI-DI Date4 Aug 2017ListedStatusListed 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  • Withdrawn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
Protemp™ Plus
Generic name
Dental material mixing nozzle
Model / Ref / Catalog
46968
Primary DI / UDI-DI
04035077004848
FDA product code
EID, EBG
GMDN term
Dental material mixing nozzle
Device class
Class I
Regulation number
872.4565, 872.3770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Temporary dental crown/bridgeDental material mixing nozzle

Other devices from 3M Deutschland GmbH

See all devices from 3M Deutschland GmbH →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: 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
  • Serial number: No
  • Manufacturing date: No