← Back to catalogue

Schlauch / Tube

EUDAMED

Class I (EU MDR)

Ref R940-5130-235

by REDA Instrumente GmbH

Identity

Device Name
Schlauch / Tube EUDAMED
Model / Reference
R940-5130-235 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058174143 EUDAMED
Basic UDI-DI
4063058000001033E EUDAMED
Direct Marketing DI
04063058174143 EUDAMED
EMDN Code
G020399 EVACUATION TUBES - OTHER 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

Schlauch / Tube 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005592

Sources (1)

  • EUDAMED f6804018-4ef0-49c8-a6c9-1bb6fa5fbacb 61 fields · synced Sep 18, 2026