Rapid Relief
by Danyang Rapid Aid Hot and Cold Therapy Products Co., Ltd 10 variants
Part of a family of 20 devices: see the family page
Ref 402
Rapid Relief (402) is a Class I device made by Danyang Rapid Aid Hot and Cold Therapy Products Co., Ltd, registered in EUDAMED on 29 Mar 2022 (Basic UDI-DI 64317reusableTY), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number64317reusableTY 00064317004021 | Date29 Mar 2022 | StatusActive |
Official records
- EUDAMED public site 64317reusableTY
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Reusable cold/hot gel compress
- Model / reference
- 402
- Primary DI / UDI-DI
- 00064317004021
- Basic UDI-DI
- 64317reusableTY
- Direct marketing DI
- 00064317004021
- EMDN code
- V9099 Various devices not included in other classes - other
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- CN-MF-000007052
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
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