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Patient Lift
EUDAMEDFDA UDIClass I (EU MDR)
Ref AY05Model AY02/AY03/AY05/AY06/AY08/AY10/AY11/AY12/AY13/AY14/AY15/AY16/AY17/AY18/AY19/AY20/AY21/AY22/AY23/AY24/AY25/AY26/AY27/AY28/AY29/AY30/AY31/AY32/AY33/AY34/AY35/AY36/AY37/AY38/AY39/AY41/AY42/AY43/AY44/AY45/AY46/AY46/AY47/AY48/AY49/AY50/AY51/AY52等Ref AY06
Identity
- Trade Name
- Patient Lift EUDAMEDVOCIC FDA UDI
- Generic Name
- Stand-assistive attendant-only-propelled wheelchair FDA UDI
- Device Name
- Patient Lift EUDAMED
- Model / Reference
- AY02/AY03/AY05/AY06/AY08/AY10/AY11/AY12/AY13/AY14/AY15/AY16/AY17/AY18/AY19/AY20/AY21/AY22/AY23/AY24/AY25/AY26/AY27/AY28/AY29/AY30/AY31/AY32/AY33/AY34/AY35/AY36/AY37/AY38/AY39/AY41/AY42/AY43/AY44/AY45/AY46/AY46/AY47/AY48/AY49/AY50/AY51/AY52等 EUDAMEDAY05 EUDAMEDAY06 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 06975960550596 EUDAMED06975960551302 EUDAMEDFDA UDI
- Basic UDI-DI
- 697596055PL001NY EUDAMED
- FDA Product Code
- FSA FDA UDI
- EMDN Code
- V0805030102 ELECTRIC MOBILE LIFTS EUDAMED
- GMDN Term
- Stand-assistive attendant-only-propelled wheelchair FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 880.5510 FDA UDI
- Market of Registration
- Germany 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Patient Lift by Zhejiang Mateside Medical Devices Technology 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 697596055PL001NY | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- EUDAMED SRN
- CN-MF-000047001
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (3)
- EUDAMED b20b0e94-7963-447c-808d-d05cfbf10528 61 fields · synced Jul 13, 2026
- FDA UDI e6db0d5f-3e29-472d-9620-eb8549b9becc 32 fields · synced May 25, 2026
- EUDAMED e1268f64-5cff-4a23-ab88-d72d2b961936 61 fields · synced Jul 13, 2026