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RayStation 9B

by Raysearch Laboratories Ab (Publ)

Ref 9.1

RayStation 9B (9.1) is a Class IIb device made by RaySearch Laboratories AB (PUBL), registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-07350002010266), active as of 7 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07350002010266 Basic UDI-DI 07350002010266UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
9.1
Primary DI / UDI-DI
07350002010266
Basic UDI-DI
B-07350002010266
EMDN code
Z11019082 Various radiotherapy and radiosurgery instruments - software accessories
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
SE-MF-000001908

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Other devices filed under VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS.

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Properties

Other properties (12, all answered No)