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Mediplus

EUDAMED

Class IIa (EU MDR)

Ref G57420181180

by Shree Umiya Surgical Pvt. Ltd

Identity

Trade Name
MEDIPLUS EUDAMED
Device Name
60 % Latex Foley Balloon Catheter - Standard Male - U2018118 EUDAMED
Model / Reference
G57420181180 EUDAMED

Identifiers

Primary DI / UDI-DI
G57420181180 EUDAMED
Basic UDI-DI
B-G57420181180 EUDAMED
EMDN Code
U010299 URETHRAL PROSTATIC AND BLADDER CATHETERS, WITH BALLOON - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Mediplus by Shree Umiya Surgical Pvt. 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
IN-MF-000018008
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ad2bad7e-3862-4d04-be99-5735ed9aa9f4 61 fields · synced Jul 25, 2026