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BioMime Aura™

EUDAMED

Class III (EU MDR)

Ref BIA222537Model Model 2

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
BioMime Aura™ EUDAMED
Device Name
BioMime Aura™ Sirolimus Eluting Coronary Stent System EUDAMED
Model / Reference
Model 2 EUDAMED
BIA222537 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224946818 EUDAMED
Basic UDI-DI
B-18904224946818 EUDAMED
EMDN Code
P070402010301 CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

BioMime Aura™ 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 3c3b13b2-3b22-4a1f-b55d-bdb0e71744b7 61 fields · synced Jun 20, 2026