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Tensi+

EUDAMED

Class I (EU MDR)

Ref PF0106

by Telic, S.A.U.

Identity

Trade Name
TENSI+ EUDAMED
Device Name
Electro-gel EUDAMED
Model / Reference
PF0106 EUDAMED

Identifiers

Primary DI / UDI-DI
03760316090092 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

Tensi+ 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 70b5b17c-56e8-40a5-87b4-8bc155160cc3 61 fields · synced Jul 25, 2026
  • EUDAMED a68b672d-83af-448d-a552-040e531ca7fb 61 fields · synced Jul 25, 2026