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BioMime Aura™

EUDAMED

Class III (EU MDR)

Ref BIA230037Model 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
BIA230037 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224947143 EUDAMED
Basic UDI-DI
B-18904224947143 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 5558268c-5b5c-482b-97a1-4cfaa9fe375b 61 fields · synced Jun 17, 2026