Skip to content

Rfh Amica-Probe

by H.S. Hospital Service S.p.A. 100 variants

Ref RFH18400E20V1

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803300334RFHAMICAPROBE7L Basic UDI-DIDate8 Jun 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  • Withdrawn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
RFH18400E20V1
Primary DI / UDI-DI
08058983743836
Basic UDI-DI
803300334RFHAMICAPROBE7L
EMDN Code
K02030101 Radiofrequency surgery electrodes, single-use
Device Class
Class IIb
Market of Registration
Italy
Medical Purpose
Termoablazione (coagulazione) di tessuti molli

Manufacturer details

EUDAMED SRN
IT-PR-000029497

Other devices from H.S. Hospital Service S.p.A.

See all devices from H.S. Hospital Service S.p.A. →

Properties

Other properties (5)

  • Sterile: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Endocrine Disruptor: No