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Suprasorb Liquacel Ag FV001039

by Speciality Fibres and Materials Limited

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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05059884011218 UDI-DI Date15 Oct 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  • Withdrawn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
Suprasorb Liquacel Ag
Generic Name
Cavity-wound management dressing, antimicrobial
Model / Ref / Catalog
FV001039, 402615
Primary DI / UDI-DI
05059884011218
FDA Product Code
FRO
GMDN Term
Cavity-wound management dressing, antimicrobial
Device Class
U
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No