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Foledrain

EUDAMED

Class IIa (EU MDR)

Ref MI/CA/01-000-EModel Foley Balloon Catheter - Latex/Silicon (2 Way/3 Way)

by Mais India Medical Devices Pvt. Ltd.

Identity

Trade Name
Foledrain EUDAMED
Device Name
Foley Balloon Catheter EUDAMED
Model / Reference
Foley Balloon Catheter - Latex/Silicon (2 Way/3 Way) EUDAMED
MI/CA/01-000-E EUDAMED

Identifiers

Primary DI / UDI-DI
08906065483975 EUDAMED
Basic UDI-DI
890606548U03NS EUDAMED
Direct Marketing DI
08906065483975 EUDAMED
EMDN Code
U0199,U020199 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Foledrain by Mais India Medical Devices Pvt. 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
IN-MF-000021842
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 20a5051a-22cc-4069-8ebf-77b70c391235 61 fields · synced Jun 19, 2026