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All Silicone Gastrostomy Balloon Catheter (Standard Type)

EUDAMED

Class IIb (EU MDR)

Ref 002 265 0180

by Create Medic Co., Ltd.

Identity

Trade Name
All Silicone Gastrostomy Balloon Catheter (Standard Type) EUDAMED
Device Name
All Silicone Gastrostomy Balloon Catheter EUDAMED
Model / Reference
002 265 0180 EUDAMED

Identifiers

Primary DI / UDI-DI
04542187229097 EUDAMED
Basic UDI-DI
45421870000893 EUDAMED
EMDN Code
G02020201 GASTROSTOMY, TUBES AND SETS EUDAMED

Classification

Device Class
Class IIb 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: Gastrostomy tube

All Silicone Gastrostomy Balloon Catheter (Standard Type) by Create Medic Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gastrostomy tube.

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 7056ad93-9ffc-4a50-b0a6-93b68eaf9ab2 61 fields · synced Jun 20, 2026