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Patient Lift

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ML-15Model 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

by Jiangmen Jia Mei Medical Products Co., Ltd.

Identity

Trade Name
Patient Lift EUDAMED
AireMed FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
Patient Lift EUDAMED
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-15 EUDAMED
AIR-15FL FDA UDI

Identifiers

Primary DI / UDI-DI
06976323220064 EUDAMEDFDA UDI
Basic UDI-DI
697632322lift44 EUDAMED
Direct Marketing DI
06976323220064 EUDAMED
FDA Product Code
FSA FDA UDI
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED
GMDN Term
Mobile patient lifting system, manual FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5510 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Patient Lift by Jiangmen Jia Mei Medical Products Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED aa734482-9fea-4ac4-a8b8-516c5b1bd774 61 fields · synced Jun 18, 2026
  • FDA UDI a6c732f4-a32e-4934-831b-d165e0529863 32 fields · synced May 30, 2026