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FLEXASOFT® C-Bogen-Beutel

EUDAMED

Class I (EU MDR)

Ref 30220

by Udo Heisig GmbH The Disposables Company

Identity

Trade Name
FLEXASOFT® C-Bogen-Beutel EUDAMED
Device Name
C-Bogen Abdeckung EUDAMED
Model / Reference
30220 EUDAMED

Identifiers

Primary DI / UDI-DI
04251806200200 EUDAMED
Basic UDI-DI
42518062004L4 EUDAMED
EMDN Code
T030101 COVER CAPS, INSTRUMENTS AND EQUIPMENT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Vascular booties

FLEXASOFT® C-Bogen-Beutel by Udo Heisig GmbH The Disposables Company — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vascular booties.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000009334

Sources (1)

  • EUDAMED df456ae9-f960-468f-847c-c5e368412766 61 fields · synced Aug 2, 2026