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Silicone Foley Catheter

EUDAMED

Class IIa (EU MDR)

Ref 91030007Model 2-way Standard: 18Fr

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
Silicone Foley Catheter EUDAMED
Device Name
Silicone Foley Catheter EUDAMED
Model / Reference
2-way Standard: 18Fr EUDAMED
91030007 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745361491 EUDAMED
Basic UDI-DI
B-06972745361491 EUDAMED
EMDN Code
U010201 URETHRAL PROSTATIC AND BLADDER CATHETERS, NELATON, WITH BALLOON EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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 812d1e14-9cb6-455f-9d22-29e17b51cad8 61 fields · synced Jun 17, 2026