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Armboard

by Reison Medical AB 2 variants

Ref 20-300

Armboard (20-300) is a Class I device made by Reison Medical Ab, registered in EUDAMED on 15 Aug 2025 (Basic UDI-DI 735011183ARMBOARDM6), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number735011183ARMBOARDM6 Basic UDI-DI 07350111833091UDI-DIDate15 Aug 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Armboard
Model / reference
20-300
Primary DI / UDI-DI
07350111833091
Basic UDI-DI
735011183ARMBOARDM6
Direct marketing DI
07350111833091
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

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

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Properties

Other properties (14, all answered No)