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Obtura™

EUDAMED

Class III (EU MDR)

Ref OBT8F

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Obtura™ EUDAMED
Device Name
Obtura™ – Vascular Closure Device EUDAMED
Model / Reference
OBT8F EUDAMED

Identifiers

Primary DI / UDI-DI
18904224918822 EUDAMED
Basic UDI-DI
B-18904224918822 EUDAMED
EMDN Code
C90010302 COLLAGEN-BASED HAEMOSTASIS SYSTEMS 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

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Obtura™ 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 ffa53293-7e65-4abc-afcd-3043d9b7576a 61 fields · synced Jun 17, 2026