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Comepa

EUDAMED

Class I (EU MDR)

Ref 3G5000US

by Telic, S.A.U.

Identity

Trade Name
Comepa EUDAMED
Device Name
Ultrasound gels EUDAMED
Model / Reference
3G5000US EUDAMED

Identifiers

Primary DI / UDI-DI
03663996018748 EUDAMED
Basic UDI-DI
8427734USGEL8L EUDAMED
EMDN Code
Z11040185 ULTRASOUND SCANNERS - CONSUMABLES 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 ffaa2835-3538-44b7-b234-d164c938a7ac 61 fields · synced Jul 17, 2026
  • EUDAMED bf50c533-523e-441e-9ae8-4b62b2d0cfbc 61 fields · synced Jul 17, 2026