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Mediplus

EUDAMED

Class IIa (EU MDR)

Ref U2018222

by Shree Umiya Surgical Pvt. Ltd

Identity

Trade Name
MEDIPLUS EUDAMED
Device Name
60 % Latex Foley Balloon Catheter - Male - U2018222 EUDAMED
Model / Reference
U2018222 EUDAMED

Identifiers

Primary DI / UDI-DI
G574U20182220 EUDAMED
Basic UDI-DI
B-G574U20182220 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

Category: Indwelling urethral drainage balloon catheter, non-antimicrobial

Mediplus by Shree Umiya Surgical Pvt. Ltd — Class IIa — MDD — 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

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Manufacturer

EUDAMED SRN
IN-MF-000018008
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED fbfe7057-5734-4ff8-99b6-be2ead6fb440 61 fields · synced Jul 23, 2026