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XA235R

by Phantom Laboratory

Ref XA235R

XA235R is a medical device (EU MDD Class I; EMDN category various bioimaging and radiotherapy instruments - hardware accessories) made by Phantom Laboratory, registered in EUDAMED on 21 Feb 2023 (Basic UDI-DI B-XA235RBK), active as of 22 Oct 2026.

Active European Union

CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-XA235RBK Basic UDI-DI D-XA235RBKUDI-DIDate21 Feb 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device name
XA235R
Model / reference
XA235R
Primary DI / UDI-DI
D-XA235RBK
Basic UDI-DI
B-XA235RBK
EMDN code
Z119080 Various bioimaging and radiotherapy instruments - hardware accessories
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
US-MF-000027490
Authorised representative
Hoff & Lowendahl AB SE-AR-000001888

Similar devices in this category

Other devices filed under VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Phantom Laboratory

See all devices from Phantom Laboratory →

Properties

  • Contains human tissues or cells
Other properties (11, all answered No)