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3M™ Snap™ STPAMP

by Kci USA, Inc.

3M™ Snap™ STPAMP is a Class II device made by Kci USA, Inc., listed in FDA GUDID since 9 Aug 2024 (UDI-DI 00849554008694), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00849554008694 UDI-DI Date9 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
3M™ Snap™
Generic name
Negative-pressure wound therapy system dressing set
Model / Ref / Catalog
STPAMP
Primary DI / UDI-DI
00849554008694
FDA product code
OKO
GMDN term
Negative-pressure wound therapy system dressing set
Device class
Class II
Regulation number
878.4683
GUDID distribution status
In Commercial Distribution

Related devices

Category: Negative-pressure wound therapy system dressing set

Other devices from Kci USA, Inc.

See all devices from Kci USA, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)