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Comepa

EUDAMED

Class I (EU MDR)

Ref 3G250EC

by Telic, S.A.U.

Identity

Trade Name
COMEPA EUDAMED
Device Name
Electro-gel EUDAMED
Model / Reference
3G250EC EUDAMED

Identifiers

Primary DI / UDI-DI
03663996018724 EUDAMED
Basic UDI-DI
8427734ECGGELVB EUDAMED
EMDN Code
C020599 CARDIAC DIAGNOSTIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Comepa by Telic, S.A.U. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Telic, S.A.U.
EUDAMED SRN
ES-MF-000001853

Sources (2)

  • EUDAMED 3b15698e-71c3-4266-9bcf-700757c96a76 61 fields · synced Jun 18, 2026
  • EUDAMED dd90deb2-4bcf-423a-88bb-7b1e2748ca6b 61 fields · synced Jun 18, 2026