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Patient Lift

by Jiangmen Jia Mei Medical Products Co., Ltd. 3 variants

Ref ML-11Model ML-5，ML-5-A，ML-5-A1，ML-5-B，ML-5-C，ML-5-D，ML-9，ML-9-A，ML-9-B，ML-9-C，ML-9-D，ML-10，ML-10-A，ML-10-B，ML-11，ML-11-B，ML-12，ML-13，ML-14，ML-15，ML-17，ML-17-A，ML-18，ML-18B，or customized

Patient Lift (ML-11) is a Class I device made by Jiangmen Jia Mei Medical Products Co., Ltd., registered in EUDAMED on 1 Dec 2025 (Basic UDI-DI 697632322lift44) and listed in FDA GUDID since 19 May 2023 (UDI-DI 06976323220040), 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
European UnionCE/MDR EUDAMED Number697632322lift44 Basic UDI-DI 06976323220040UDI-DIDate1 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number06976323220040 UDI-DI Date19 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 697632322lift44 registered 1 Dec 2025 Active
  • FDA GUDID UDI-DI 06976323220040 listed 19 May 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 06976323220040
  2. Registered EUDAMED 697632322lift44

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  • Withdrawn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
Patient Lift EUDAMED
AireMed GUDID
Generic name
Mobile patient lifting system, manual
Model / reference
ML-5，ML-5-A，ML-5-A1，ML-5-B，ML-5-C，ML-5-D，ML-9，ML-9-A，ML-9-B，ML-9-C，ML-9-D，ML-10，ML-10-A，ML-10-B，ML-11，ML-11-B，ML-12，ML-13，ML-14，ML-15，ML-17，ML-17-A，ML-18，ML-18B，or customized EUDAMED
ML-11 EUDAMED
AIR-11HL GUDID
Primary DI / UDI-DI
06976323220040
Basic UDI-DI
697632322lift44
Direct marketing DI
06976323220040
FDA product code
FSA
EMDN code
V0805030101 Manual mobile lifts
GMDN term
Mobile patient lifting system, manual
Device class
Class I
Regulation number
880.5510
EU registration type
Standard device
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
CN-MF-000010529
Authorised representative
Sungo Cert GmbH DE-AR-000010869

Other devices from Jiangmen Jia Mei Medical Products Co., Ltd.

See all devices from Jiangmen Jia Mei Medical Products Co., Ltd. →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (23, all answered No)