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3M™ Adaptic™ TCH502

by 3M Company

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04054596951730 UDI-DI Date21 Apr 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  • Withdrawn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
3M™ Adaptic™
Generic Name
Wound-nonadherent dressing, permeable, non-antimicrobial
Model / Ref / Catalog
TCH502
Primary DI / UDI-DI
04054596951730
FDA Product Code
NAD
GMDN Term
Wound-nonadherent dressing, permeable, non-antimicrobial
Device Class
Class I
Regulation Number
878.4020
GUDID distribution status
In Commercial Distribution

Other devices from 3M Company

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No