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Dafodil™ Pericardial Bioprosthesis Valve

EUDAMED

Class III (EU MDR)

Ref PBMSS2333Ref PBASS1929

by Meril Life Sciences Pvt. Ltd.

Identity

Device Name
Dafodil™ Pericardial Bioprosthesis Valve EUDAMED
Model / Reference
PBMSS2333 EUDAMED
PBASS1929 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224958194 EUDAMED
18904224973579 EUDAMED
Basic UDI-DI
89042249PBE8 EUDAMED
Direct Marketing DI
18904224958194 EUDAMED
18904224973579 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 (2)

  • EUDAMED 16011b2b-5d0e-4edb-becd-0e630ffac797 61 fields · synced Aug 4, 2026
  • EUDAMED 14b84d4d-b494-4a2c-907f-1841b26d289a 61 fields · synced May 17, 2026