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Mammoth™

EUDAMED

Class III (EU MDR)

Ref MTV2040

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Mammoth™ EUDAMED
Device Name
Mammoth™ Balloon Dilatation Catheter EUDAMED
Model / Reference
MTV2040 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224926148 EUDAMED
Basic UDI-DI
B-18904224926148 EUDAMED
EMDN Code
C019014 CARDIAC VALVULOPLASTY CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Austria 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

Mammoth™ by Meril Life Sciences Pvt. Ltd. — Class III — 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-000008308
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 13b5e5d9-958e-4e16-bdae-acd9713cb4e8 61 fields · synced Jul 24, 2026