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Dilatator / Dilators, other

EUDAMED

Class I (EU MDR)

Ref 71438-13

by REDA Instrumente GmbH

Identity

Device Name
Dilatator / Dilators, other EUDAMED
Model / Reference
71438-13 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058056692 EUDAMED
Basic UDI-DI
4063058000000183N EUDAMED
Direct Marketing DI
04063058056692 EUDAMED
EMDN Code
L070802 VASCULAR DILATORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Dilatator / Dilators, other by REDA Instrumente GmbH — 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

EUDAMED SRN
DE-MF-000005592

Sources (1)

  • EUDAMED 938e2727-d11b-4681-8388-3b399bb17b70 61 fields · synced Sep 18, 2026