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Cocoon

EUDAMED

Class III (EU MDR)

Ref CPF25

by Vascular Innovations Co. Ltd.

Identity

Trade Name
Cocoon EUDAMED
Device Name
Cocoon PFO Occluders EUDAMED
Model / Reference
CPF25 EUDAMED

Identifiers

Primary DI / UDI-DI
08858788500678 EUDAMED
Basic UDI-DI
B-08858788500678 EUDAMED
EMDN Code
P07040303 CARDIAC OCCLUDERS, FORAMEN OVALE AND BOTALLO DUCT EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Spain 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

Cocoon by Vascular Innovations Co. Ltd. — Class III — CE/MDR — 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
TH-MF-000028144
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 4b847a4a-cbc1-48b0-8e67-ba04519529b0 61 fields · synced Oct 6, 2026