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Epicutaneo-Cava Catheter 2184.015

by VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG

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 Number03660812013444 UDI-DI Date27 Oct 2015ListedStatusListed 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  • Withdrawn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
Epicutaneo-Cava Catheter
Generic Name
Peripherally-inserted central venous catheter
Model / Ref / Catalog
2184.015
Primary DI / UDI-DI
03660812013444
FDA Product Code
LJS
GMDN Term
Peripherally-inserted central venous catheter
Device Class
Class II
Regulation Number
880.5970
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripherally-inserted central venous catheter

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Lot / Batch Number
  • Serial Number

Other properties (9)

  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No
  • Manufacturing Date: No