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Infusion Transfer System

by Maquet (Suzhou) Co., Ltd 2 variants

Ref M-ShiftModel M-SHIFT

Infusion Transfer System (M-Shift) is an intravenous track/carrier system (EU MDR Class I; FDA Class I; FDA product code FOX, Stand, Infusion) made by Maquet (Suzhou) Co., Ltd, registered in EUDAMED on 17 Nov 2021 (Basic UDI-DI 69702831306AHK) and listed in FDA GUDID since 7 Dec 2022 (UDI-DI 06970283130814), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06970283130814 UDI-DI Date7 Dec 2022ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number69702831306AHK Basic UDI-DI 06970283130814UDI-DIDate17 Nov 2021RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 69702831306AHK registered 17 Nov 2021 Active
  • FDA GUDID UDI-DI 06970283130814 listed 7 Dec 2022 Listed

Timeline

2 dated events

  1. Registered EUDAMED 69702831306AHK
  2. Listed FDA GUDID 06970283130814

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  • Withdrawn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

Generic name
Intravenous track/carrier system
Model / reference
M-SHIFT
Primary DI / UDI-DI
06970283130814
Basic UDI-DI
69702831306AHK
FDA product code
FOX
EMDN code
Z129007 Hanging units for the operating room and intensive care
GMDN term
Intravenous track/carrier system
Device class
Class I
Regulation number
880.6990
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
CN-MF-000016104
Authorised representative
MAQUET GmbH DE-AR-000009120

Similar devices in this category

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)