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Axiom P

by Ki Mobility LLC 44 variants

Part of a family of 1,571 devices: see the family page

Ref XP1717C2Model Seating

Axiom P (XP1717C2) is a Class I device made by Ki Mobility, LLC, registered in EUDAMED on 21 Aug 2025 (Basic UDI-DI 08403633SEATINGK7), 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 Number08403633SEATINGK7 Basic UDI-DI 00840363376981UDI-DIDate21 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  • Withdrawn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

Model / reference
Seating, XP1717C2
Primary DI / UDI-DI
00840363376981
Basic UDI-DI
08403633SEATINGK7
EMDN code
V080399 Medical cushions - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
US-MF-000012633
Authorised representative
Etac Supply Center AB SE-AR-000001601

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Properties

Other properties (14, all answered No)