Electric Bed
by Jiangmen Jia Mei Medical Products Co., Ltd. 10 variants
Ref MBE-3XEModel MBE-1XX,MBE-1XX-A,MBE-1XX-D,MBE-1XXG,MBE-2AB,MBE-2ABA,MBE-2ABG,MBE-2CB-D,MBE-2CB-E,MBE-2CB-F,MBE-2CDG,MBE-2CX,MBE-2CX-A,MBE-2CX-B,MBE-2CX-C,MBE-2XX,etc
Electric Bed (MBE-3XE) is a device classified as Class I in the EU and Class II in the US made by Jiangmen Jia Mei Medical Products Co., Ltd., registered in EUDAMED on 13 Nov 2025 (Basic UDI-DI 697632322electricbedEH) and listed in FDA GUDID since 19 May 2023 (UDI-DI 06976323220002), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number697632322electricbedEH 06976323220002 | Date13 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number06976323220002 | Date19 May 2023 | StatusListed |
Official records
- EUDAMED public site 697632322electricbedEH
- AccessGUDID record 06976323220002
Across registries
- EUDAMED Basic UDI-DI 697632322electricbedEH registered 13 Nov 2025 Active
- FDA GUDID UDI-DI 06976323220002 listed 19 May 2023 Listed
Timeline
- Listed FDA GUDID 06976323220002
- Registered EUDAMED 697632322electricbedEH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Electric Bed EUDAMEDAireMed GUDID
- Generic name
- Basic electric hospital bed
- Model / reference
- MBE-1XX,MBE-1XX-A,MBE-1XX-D,MBE-1XXG,MBE-2AB,MBE-2ABA,MBE-2ABG,MBE-2CB-D,MBE-2CB-E,MBE-2CB-F,MBE-2CDG,MBE-2CX,MBE-2CX-A,MBE-2CX-B,MBE-2CX-C,MBE-2XX,etc EUDAMEDMBE-3XE EUDAMEDAIR-36XE GUDID
- Primary DI / UDI-DI
- 06976323220002
- Basic UDI-DI
- 697632322electricbedEH
- Direct marketing DI
- 06976323220002
- FDA product code
- FNL
- EMDN code
- V08060101 Hospital/home care electric medical beds
- GMDN term
- Basic electric hospital bed
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 880.5100
- EU registration type
- Standard device
- EU market of registration
- Austria
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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. →