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Covrsite 59714000

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00040565117690 UDI-DI Date19 Jan 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  • Withdrawn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
Covrsite
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Ref / Catalog
59714000, 59714000 / 59714100
Primary DI / UDI-DI
00040565117690
FDA Product Code
KGX
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device Class
Class I
Regulation Number
880.5240
GUDID distribution status
In Commercial Distribution
Size
Width — 10 Centimeter
Length — 10 Centimeter

Other devices from Smith & Nephew Medical, Ltd.

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

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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