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Solventum™ Promogran™ PG004

by Solventum Germany GmbH

Solventum™ Promogran™ PG004 is a device classified as Unclassified made by Solventum Germany GmbH, listed in FDA GUDID since 22 Sep 2025 (UDI-DI 00197998275340), 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 Number00197998275340 UDI-DI Date22 Sep 2025ListedStatusListed 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  • Withdrawn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
Solventum™ Promogran™
Generic name
Animal-derived wound matrix dressing
Model / Ref / Catalog
PG004
Primary DI / UDI-DI
00197998275340
FDA product code
KGN
GMDN term
Animal-derived wound matrix dressing
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Animal-derived wound matrix dressing

Other devices from Solventum Germany GmbH

See all devices from Solventum Germany GmbH →

Properties

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