Skip to content

Medi-Vac 65652-135

by Cardinal Health 200, LLC

Part of a family of 13 devices: see the family page

Ref 65652-135Model Ring Brackets

Medi-Vac 65652-135 is a device classified as Class I in the EU and Class II in the US made by Cardinal Health 200, LLC, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 0630140000000000000003363) and listed in FDA GUDID since 6 Mar 2018 (UDI-DI 10630140153105), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0630140000000000000003363 Basic UDI-DI 10630140153105UDI-DIDate8 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10630140153105 UDI-DI Date6 Mar 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0630140000000000000003363 registered 8 Oct 2026 Active
  • FDA GUDID UDI-DI 10630140153105 listed 6 Mar 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10630140153105
  2. Registered EUDAMED 0630140000000000000003363

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  • Withdrawn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
Medi-Vac
Generic name
Suction/irrigation system canister/bottle holder, reusable
Device name
Ring Brackets
Model / Ref / Catalog
65652-135, Ring Brackets
Primary DI / UDI-DI
10630140153105
Basic UDI-DI
0630140000000000000003363
Direct marketing DI
10630140153105
FDA product code
GCX
EMDN code
A06030499 Intra-operation fluid collection devices - other
GMDN term
Suction/irrigation system canister/bottle holder, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Standard device
EU market of registration
Ireland
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.

Similar devices in this category

Other devices filed under INTRA-OPERATION FLUID COLLECTION DEVICES - OTHER.

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)