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Vygon 9888.002

by Vygon

Ref 9888.002

Vygon 9888.002 (009888002) is a device classified as Class I in the EU and Class II in the US made by Vygon, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI B-03660812040617) and listed in FDA GUDID since 21 Jun 2021 (UDI-DI 03660812040617), active as of 9 Nov 2026.

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

CE MDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-03660812040617 Basic UDI-DI 03660812040617UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03660812040617 UDI-DI Date21 Jun 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-03660812040617 registered 15 Oct 2026 Active
  • FDA GUDID UDI-DI 03660812040617 listed 21 Jun 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03660812040617
  2. Registered EUDAMED B-03660812040617

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  • Withdrawn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
Dualstopwhite ♂/♀ EUDAMED
Vygon GUDID
Generic name
Catheter orifice occluder
Model / Ref / Catalog
9888.002, 009888002
Primary DI / UDI-DI
03660812040617
Basic UDI-DI
B-03660812040617
FDA product code
DQO
EMDN code
A070501 Caps or obturators, non-perforable
GMDN term
Catheter orifice occluder
Device class
Class I EUDAMED
Class II GUDID
Regulation number
870.1200
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Catheter orifice occluder

Similar devices in this category

Other devices filed under CAPS OR OBTURATORS, NON-PERFORABLE.

Other devices from Vygon

See all devices from Vygon →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)