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Mozec™

EUDAMED

Class III (EU MDR)

Ref MOZD27525

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Mozec™ EUDAMED
Device Name
Mozec™ - Rx PTCA Balloon Dilatation Catheter EUDAMED
Model / Reference
MOZD27525 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224952796 EUDAMED
Basic UDI-DI
B-18904224952796 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

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

Category: Coronary angioplasty balloon catheter, cutting/scoring

Mozec™ by Meril Life Sciences Pvt. Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000008308
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 5d5896c5-c4ae-458b-b323-95b1f46430aa 61 fields · synced Jun 9, 2026