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VIVA RF Electrode

by STARMED Co., Ltd. 19 variants

Ref 18-10V05-30X

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

21 Feb 2029

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberKR24/00000016 Date28 Apr 2026IssuedStatusActive expires 21 Feb 2029
European UnionCE/MDD EUDAMED Number880930676VIVA_EWD Basic UDI-DI 08809306761323UDI-DIDate22 May 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number08809306761323 UDI-DI Date9 Apr 2021ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • KR24/00000016 Active Supplemented

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    28 Apr 2026
    Expires
    21 Feb 2029
    Reason
    Change approved

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
Model / Reference
18-10V05-30X
Primary DI / UDI-DI
08809306761323
Basic UDI-DI
880930676VIVA_EWD, B-08809306761323
FDA Product Code
GEI
EMDN Code
K0201010301 Open electrosurgery electrodes, single-use
GMDN Term
Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
878.4400
EU market of registration
Bulgaria
France
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 18 Gauge
Length — 10 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

Manufacturer details

EUDAMED SRN
KR-MF-000008605
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Related devices

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Other devices from Starmed Co., Ltd

See all devices from Starmed Co., Ltd →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No