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bio-UMAXX 100% SILIKON FOLEY KATHETER

EUDAMED

Class IIb (EU MDR)

Ref FC20230DModel FC06201DP

by Integral Medical Products Co., Ltd.

Identity

Trade Name
bio-UMAXX 100% SILIKON FOLEY KATHETER EUDAMED
Device Name
Silicone Foley Catheter EUDAMED
Model / Reference
FC06201DP EUDAMED
FC20230D EUDAMED

Identifiers

Primary DI / UDI-DI
06970675357409 EUDAMED
Basic UDI-DI
697067535IMP2BSNNNSFC00VE EUDAMED
B-06970675357409 EUDAMED
EMDN Code
U010299 URETHRAL PROSTATIC AND BLADDER CATHETERS, WITH BALLOON - OTHER EUDAMED

Classification

Device Class
Class IIb 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: Indwelling urethral drainage balloon catheter, non-antimicrobial

bio-UMAXX 100% SILIKON FOLEY KATHETER by Integral Medical Products Co., Ltd. — Class IIb — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Indwelling urethral drainage balloon catheter, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000009217
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 2db028e2-0d35-44cb-935f-e5197150d65a 61 fields · synced Jul 17, 2026
  • EUDAMED 31c199f5-f634-4269-ae34-8e50cf4d4a65 61 fields · synced Jul 17, 2026