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Uresil Evolution PRE.VAC WOUND DRAINAGE BOTTLE 1000 mL ESB-1001SP

by Canadian Hospital Specialties 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04719899159787 UDI-DI Date18 Aug 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  • Withdrawn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
Uresil Evolution PRE.VAC WOUND DRAINAGE BOTTLE 1000 mL
Generic Name
Closed-wound/centesis drainage receptacle
Model / Ref / Catalog
ESB-1001SP
Primary DI / UDI-DI
04719899159787
FDA Product Code
GCY
GMDN Term
Closed-wound/centesis drainage receptacle
Device Class
Class I
Regulation Number
878.4680
GUDID distribution status
In Commercial Distribution

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Properties

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

Other properties (9)

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