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Scotchbond™ Universal 41292

by 3M Deutschland GmbH 2 variants

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 Number04035077010672 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  • Withdrawn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
Scotchbond™ Universal
Generic Name
Dentine bonding agent/set
Model / Ref / Catalog
41292
Primary DI / UDI-DI
04035077010672
FDA Product Code
KLE
GMDN Term
Dentine bonding agent/set
Device Class
Class II
Regulation Number
872.3200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dentine bonding agent/set

Other devices from 3M Deutschland GmbH

See all devices from 3M Deutschland GmbH →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: 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