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Mordedor-Mo

EUDAMED

Class I (EU MDR)

Ref 7600

by Telic, S.A.U.

Identity

Trade Name
MORDEDOR-MO EUDAMED
Device Name
Bite-blocks EUDAMED
Model / Reference
7600 EUDAMED

Identifiers

Primary DI / UDI-DI
08427734001936 EUDAMED
Basic UDI-DI
8427734BITEBLOCKKW EUDAMED
EMDN Code
R0199 INTUBATION 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

Mordedor-Mo 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 dbff98f0-4b07-401e-84db-ac921f9ab14a 61 fields · synced Jun 18, 2026
  • EUDAMED 45332140-ac5e-44dd-9746-6b513498d7f3 61 fields · synced Jun 18, 2026