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Rfh Amica-Probe

by H.S. Hospital Service S.p.A. EUDAMED

Active European Union

Ref RFH18070E07V2-W1

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803300334RFHAMICAPROBE7L Basic UDI-DIDate8 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

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.

Specification

EUDAMED

Model / Reference
RFH18070E07V2-W1
Primary DI / UDI-DI
08058983746004
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