Skip to content

Theranojet ARA

by Lemer Pax

Ref 00055989Model Theranojet ARA

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3701430100055989TL Basic UDI-DI 03701430101059UDI-DIDate14 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Theranojet ARA, 00055989
Primary DI / UDI-DI
03701430101059
Basic UDI-DI
3701430100055989TL
EMDN Code
Z11029099 Various instruments for nuclear medicine - other
Device Class
Class IIb
Medical Purpose
The THERANOJET®ARA is used for intravenous infusion of radiopharmaceuticals for theranostic purposes, in compliance with the pump's intended use.

Manufacturer details

EUDAMED SRN
FR-PR-000042149

Other devices from Lemerpax

See all devices from Lemerpax →

Properties

Other properties (1)

  • Sterile: No