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Ekisu

EUDAMED

Class III (EU MDR)

Ref EKS6F

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Ekisu EUDAMED
Device Name
Ekisu Aspiration Catheter EUDAMED
Model / Reference
EKS6F EUDAMED

Identifiers

Primary DI / UDI-DI
18904224938592 EUDAMED
Basic UDI-DI
B-18904224938592 EUDAMED
EMDN Code
C010401020501 MANUAL CARDIAC THROMBECTOMY AND THROMBOASPIRATION SYSTEMS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Ekisu 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 5f6c24e6-0b95-4fe5-83e6-4b7f0d64065b 61 fields · synced Aug 4, 2026