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Vygon 812.000

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

Ref 812.000

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-03660812124492 Basic UDI-DI 03660812124492UDI-DIDate12 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03660812124492 UDI-DI Date9 Jun 2021ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
repairset for epicutaneo cava pur EUDAMED
Vygon GUDID
Generic Name
Intravenous administration tubing extension set
Model / Ref / Catalog
812.000, 000812000
Primary DI / UDI-DI
03660812124492
Basic UDI-DI
B-03660812124492
FDA Product Code
LJS
EMDN Code
C01020101 Central i.v. single-lumen catheters, peripheral access
GMDN Term
Intravenous administration tubing extension set
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
880.5970
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Intravenous administration tubing extension set

Other devices from VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (17)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No