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Silicone Foley Catheter

EUDAMED

Class IIa (EU MDR)

Ref 91030018Model 3-way Standard: 24Fr

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
Silicone Foley Catheter EUDAMED
Device Name
Silicone Foley Catheter EUDAMED
Model / Reference
3-way Standard: 24Fr EUDAMED
91030018 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745361637 EUDAMED
Basic UDI-DI
B-06972745361637 EUDAMED
EMDN Code
U010201 URETHRAL PROSTATIC AND BLADDER CATHETERS, NELATON, WITH BALLOON EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Silicone Foley Catheter by Guangzhou Orcl Medical Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000039222
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED e69b23b3-6e51-4b74-bd01-55668522078d 61 fields · synced Jun 18, 2026