Armboard
by Reison Medical AB 2 variants
Ref 20-300-10
Armboard (20-300-10) is a Class I device made by Reison Medical Ab, registered in EUDAMED on 15 Aug 2025 (Basic UDI-DI 735011183ARMBOARDM6), active as of 23 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 | Number735011183ARMBOARDM6 07350111833107 | Date15 Aug 2025 | StatusActive |
Official records
- EUDAMED public site 735011183ARMBOARDM6
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- Withdrawn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
- Armboard
- Model / reference
- 20-300-10
- Primary DI / UDI-DI
- 07350111833107
- Basic UDI-DI
- 735011183ARMBOARDM6
- Direct marketing DI
- 07350111833107
- EMDN code
- Z12011299 Patient positioning instruments – other
- Device class
- Class I
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Sweden
Manufacturer details
- EUDAMED SRN
- SE-MF-000002468
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