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Proplate

by Bio Protech Inc. 80 variants

Part of a family of 86 devices: see the family page

Ref 9642F

Proplate (9642F) is a medical device (EU MDR Class IIb; EMDN category electrosurgery dual patient pads (neutral electrodes)) made by Bio Protech Inc., registered in EUDAMED on 13 Aug 2026 (Basic UDI-DI 880908394090L4), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880908394090L4 Basic UDI-DI 08809083945657UDI-DIDate13 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Electrosurgical Grounding Plate
Model / reference
9642F
Primary DI / UDI-DI
08809083945657
Basic UDI-DI
880908394090L4
EMDN code
K02010202 Electrosurgery dual patient pads (neutral electrodes), single-use
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

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

Similar devices in this category

Other devices filed under ELECTROSURGERY DUAL PATIENT PADS (NEUTRAL ELECTRODES), SINGLE-USE.

Other devices from Bio Protech Inc.

See all devices from Bio Protech Inc. →

Properties

Other properties (14, all answered No)