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Menox

EUDAMED

Class III (EU MDR)

Ref MNX20

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Menox EUDAMED
Device Name
Menox Liquid Embolic System EUDAMED
Model / Reference
MNX20 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224927183 EUDAMED
Basic UDI-DI
B-18904224927183 EUDAMED
EMDN Code
N0199 ENCEPHALIC AND PERIPHERAL NERVOUS SYSTEM DEVICES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Menox 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 a929aa4f-d2ce-4c31-a65f-e759d74e8c05 61 fields · synced Jun 19, 2026