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Suprasorb 90x150(50x105)mm

by Huizhou Foryou Medical Devices Co., Ltd.

Suprasorb 90x150(50x105)mm (139087) is a Class I device made by Huizhou Foryou Medical Devices Co., Ltd., listed in FDA GUDID since 29 Aug 2024 (UDI-DI 06940610115104), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06940610115104 UDI-DI Date29 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  • Withdrawn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
Suprasorb
Generic name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Ref / Catalog
90x150(50x105)mm, 139087
Primary DI / UDI-DI
06940610115104
FDA product code
NAD
GMDN term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device class
Class I
Regulation number
878.4020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

Other devices from Huizhou Foryou Medical Devices Co., Ltd.

See all devices from Huizhou Foryou Medical Devices Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)