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Nexgen™

EUDAMED

Class III (EU MDR)

Ref NXG27540Model Model 1

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Nexgen™ EUDAMED
Device Name
NexGen™ Cobalt Chromium Coronary Stent System EUDAMED
Model / Reference
Model 1 EUDAMED
NXG27540 EUDAMED

Identifiers

Primary DI / UDI-DI
18906029350272 EUDAMED
Basic UDI-DI
B-18906029350272 EUDAMED
EMDN Code
P070402010102 METALLIC NON-STAINLESS STEEL CORONARY STENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

Nexgen™ 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 2776b7c0-58ce-4ceb-a19e-a84d2a434ef1 61 fields · synced Jun 19, 2026