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Kinder Plus

EUDAMED

Class IIa (EU MDR)

Ref KKN1735E8090

by Biopsybell Srl

Identity

Trade Name
KINDER PLUS EUDAMED
Device Name
KINDER PLUS EUDAMED
Model / Reference
KKN1735E8090 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860030667 EUDAMED
Basic UDI-DI
B-08033860030667 EUDAMED
EMDN Code
U08020201 SINGLE LUMEN NEEDLES AND SETS/SYSTEMS FOR OOCYTE RETRIEVAL EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Kinder Plus by Biopsybell Srl — Class IIa — 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

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED c40195ea-7593-4d09-9065-8fc8eaec9952 61 fields · synced Jul 10, 2026