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CentriMag™ 201-50112

by Thoratec Corporation

Ref 201-50112Model ZMOD-201-50112

CentriMag 201-50112 is a portable active medical device mount (EU MDR Class I; FDA Class I; FDA product code KRI, Accessory Equipment, Cardiopulmonary Bypass) made by Thoratec Corporation, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI 081302401CMG0009HJ) and listed in FDA GUDID since 29 Mar 2022 (UDI-DI 07640135140283), 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 Number081302401CMG0009HJ Basic UDI-DI 07640135140283UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640135140283 UDI-DI Date29 Mar 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081302401CMG0009HJ registered 15 Oct 2026 Active
  • FDA GUDID UDI-DI 07640135140283 listed 29 Mar 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07640135140283
  2. Registered EUDAMED 081302401CMG0009HJ

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  • Withdrawn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
CentriMag™
Generic name
Portable active medical device mount
Device name
CentriMag Motor Bracket
Model / Ref / Catalog
201-50112, ZMOD-201-50112
Primary DI / UDI-DI
07640135140283
Basic UDI-DI
081302401CMG0009HJ
FDA product code
KRI
EMDN code
C030180 Extracorporeal and assisted circulation devices - accessories
GMDN term
Portable active medical device mount
Device class
Class I
Regulation number
870.4200
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Related devices

Category: Portable active medical device mount

Similar devices in this category

Other devices filed under EXTRACORPOREAL AND ASSISTED CIRCULATION DEVICES - ACCESSORIES.

Other devices from Thoratec Corporation

See all devices from Thoratec Corporation →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)