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Proplate

by Bio Protech Inc. South Korea EUDAMED

Ref P9642F

EMDN K02010202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880908394090L4 Basic UDI-DIDate13 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Electrosurgical Grounding Plate
Model / Reference
P9642F
Primary DI / UDI-DI
08809083945695
Basic UDI-DI
880908394090L4
EMDN Code
K02010202 Electrosurgery dual patient pads (neutral electrodes), single-use
Device Class
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000012687
Authorised representative
Meridius Medical Europe Limited IE-AR-000004258

Other devices from Bio Protech Inc.

See all devices from Bio Protech Inc. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • 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

Sources (1)

  • EUDAMED 08809083945695|880908394090L4 61 fields · synced 24 Oct 2026