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VeinCLEAR™ Generator V-700

by RF Medical Co., Ltd.

Ref V-700

VeinCLEAR™ Generator V-700 is a Class IIb device made by RF Medical Co., Ltd., registered in EUDAMED on 27 Jul 2026 (Basic UDI-DI 880014291603BB) with CE/MDR certificate KR23/00000154 valid until 21 Sep 2028, active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

21 Sep 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880014291603BB Basic UDI-DI 08809295147078UDI-DIDate27 Jul 2026RegisteredStatusActive

Official records

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • KR23/00000154 Active Supplemented

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    23 Apr 2026
    Expires
    21 Sep 2028
    Reason
    Other

Timeline

3 dated events

  1. Certificate issued EUDAMED KR23/00000154
  2. Registered EUDAMED 880014291603BB
  3. Certificate expires EUDAMED KR23/00000154

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
V-700
Primary DI / UDI-DI
08809295147078
Basic UDI-DI
880014291603BB
EMDN code
Z12010902 Electrosurgical units (esu) for general use
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
KR-MF-000012647
Authorised representative
Obelis s.a. BE-AR-000000106

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Properties

Other properties (14, all answered No)