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Kit Radiofrequenza Nimbus® Mini

by Advanced Medical Systems Group S.R.L. 3 variants

Ref AMS/NB150-10-M

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 Number805424725KITRFNBRD Basic UDI-DI 08054247255220UDI-DIDate1 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  • Withdrawn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

Device Name
Sistema Nimbus per procedure di radiofrequenza
Model / Reference
AMS/NB150-10-M
Primary DI / UDI-DI
08054247255220
Basic UDI-DI
805424725KITRFNBRD
EMDN Code
K020399 Devices for surgery with radiofrequency generator, single-use - other
Device Class
Class III
Medical Purpose
Il sistema Nimbus per procedure di radiofrequenza è indicato per le procedure di lesione termica, tramite radiofrequenza pulsata (PRF) o radiofrequenza standard (RF), delle terminazioni nervose periferiche per il trattamento e il controllo del dolore cronico e acuto.

Manufacturer details

EUDAMED SRN
IT-PR-000058313

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Properties

Other properties (1)

  • Sterile: No