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Transanale Dekompressionssonde

EUDAMED

Class IIa (EU MDR)

Ref DDABA03503

by Create Medic Co., Ltd.

Identity

Trade Name
Transanale Dekompressionssonde EUDAMED
Device Name
Transanal Ileus Decompression Tube Set EUDAMED
Model / Reference
DDABA03503 EUDAMED

Identifiers

Primary DI / UDI-DI
04542187172607 EUDAMED
Basic UDI-DI
4542187000078Z EUDAMED
EMDN Code
G0301010501 COLONIC BALLOON CATHETERS, LOW PRESSURE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Transanale Dekompressionssonde by Create Medic Co., Ltd. — Class IIa — 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
JP-MF-000010849
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 55b1afbc-7c12-40ca-9c4d-7bd80c67570d 61 fields · synced Jun 19, 2026