Skip to content

Vide ST423-0001

by Alleva Medical Limited

Ref ST423-0001

Vide ST423-0001 is a thoracic suction collection container (EU MDR Class I; FDA Class II; FDA product code KDQ, Bottle, Collection, Vacuum) made by Alleva Medical Limited, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 489708907ST423PR) and listed in FDA GUDID since 11 Dec 2023 (UDI-DI 04897089070989), active as of 12 Nov 2026.

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

CE MDR

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number489708907ST423PR Basic UDI-DI 04897089070989UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04897089070989 UDI-DI Date11 Dec 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 489708907ST423PR registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04897089070989 listed 11 Dec 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04897089070989
  2. Registered EUDAMED 489708907ST423PR

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Vide® Dual Chamber Dry Suction Water Seal Chest Drain EUDAMED
Vide GUDID
Generic name
Thoracic suction collection container
Device name
Vide® Dual Chamber Dry Suction/Water Seal Chest Drain
Model / Ref / Catalog
ST423-0001
Primary DI / UDI-DI
04897089070989
Basic UDI-DI
489708907ST423PR
Direct marketing DI
04897089070989
FDA product code
KDQ
EMDN code
A0601010201 Drainage systems with adjustable suction and collection chamber
GMDN term
Thoracic suction collection container
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 04897089070989: EUDAMED states No, FDA GUDID states Yes.

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: Thoracic suction collection container

Similar devices in this category

Other devices filed under DRAINAGE SYSTEMS WITH ADJUSTABLE SUCTION AND COLLECTION CHAMBER.

Other devices from Alleva Medical Limited

See all devices from Alleva Medical Limited →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Measuring function
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (16, all answered No)