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DURAMAX S Silicone super absorbent dressing 66023134

by Smith & Nephew Medical, Ltd.

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 Number05000223500856 UDI-DI Date29 Jun 2022ListedStatusListed 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  • Withdrawn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
DURAMAX S Silicone super absorbent dressing
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Ref / Catalog
66023134
Primary DI / UDI-DI
05000223500856
FDA Product Code
NAC
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device Class
Class I
Regulation Number
878.4018
GUDID distribution status
In Commercial Distribution

Related devices

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

Other devices from Smith & Nephew Medical, Ltd.

See all devices from Smith & Nephew Medical, Ltd. →

Properties

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

Other properties (9)

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