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Desfi-Dormo

EUDAMED

Class IIa (EU MDR)

Ref VE-022

by Telic, S.A.U.

Identity

Trade Name
DESFI-DORMO EUDAMED
Device Name
Vein strippers EUDAMED
Model / Reference
VE-022 EUDAMED

Identifiers

Primary DI / UDI-DI
08427734035382 EUDAMED
Basic UDI-DI
8427734VEINSTRIPPERSZP EUDAMED
EMDN Code
C0699 CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Surgical bulldog clamp, single-use

Desfi-Dormo by Telic, S.A.U. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

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 93994cf1-80db-4db1-99a7-7cbd61eeff52 61 fields · synced Jul 12, 2026
  • EUDAMED 2b100c4a-d588-4f16-9102-208ca52b08e6 61 fields · synced Jun 14, 2026