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Kanüle, Absaugung / Cannula, suction

EUDAMED

Class IIa (EU MDR)

Ref 41295-05

by REDA Instrumente GmbH

Identity

Device Name
Kanüle, Absaugung / Cannula, suction EUDAMED
Model / Reference
41295-05 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058239811 EUDAMED
Basic UDI-DI
4063058000001864C EUDAMED
Direct Marketing DI
04063058239811 EUDAMED
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE EUDAMED

Classification

Device Class
Class IIa 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

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Kanüle, Absaugung / Cannula, suction by REDA Instrumente GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

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 b5001226-4358-431f-83a2-9c65a282b88a 61 fields · synced Jun 19, 2026