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Medikas

by Telic, S.A.U. 7 variants

Part of a family of 48 devices: see the family page

Ref 2700Model 2125-C/00

Medikas (2700) is a Class IIb device made by Telic, S.A.U., registered in EUDAMED on 26 Jan 2026 (Basic UDI-DI 8427734ESUPLATES3L), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8427734ESUPLATES3L Basic UDI-DI 08427734010679UDI-DIDate26 Jan 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
2125-C/00, 2700
Primary DI / UDI-DI
08427734010679
Basic UDI-DI
8427734ESUPLATES3L
EMDN code
K02010202 Electrosurgery dual patient pads (neutral electrodes), single-use
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001853

Related devices

Category: Electrosurgical return electrode, single-use

Similar devices in this category

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

Other devices from Telic, S.A.U.

See all devices from Telic, S.A.U. →

Properties

Other properties (14, all answered No)