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Dafodil™ Pericardial Bioprosthesis Valve

EUDAMED

Class III (EU MDR)

Ref PBMSS2331

by Meril Life Sciences Pvt. Ltd.

Identity

Device Name
Dafodil™ Pericardial Bioprosthesis Valve EUDAMED
Model / Reference
PBMSS2331 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224958170 EUDAMED
Basic UDI-DI
89042249PBE8 EUDAMED
Direct Marketing DI
18904224958170 EUDAMED
EMDN Code
P07038001 HEART VALVE IMPLANT SIZERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Heart valve annulus sizer, reusable

Dafodil™ Pericardial Bioprosthesis Valve by Meril Life Sciences Pvt. Ltd. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Heart valve annulus sizer, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000008308
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 92d83f54-3b86-48f4-9354-7f951f5f4cee 61 fields · synced Jun 18, 2026