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IDkit Hp® Two

EUDAMED

Class I (EU MDR)

Ref AC00050

by Meridian Bioscience Israel Ltd.

Identity

Trade Name
IDkit Hp® Two EUDAMED
Device Name
IDkit Hp® Two EUDAMED
Model / Reference
AC00050 EUDAMED

Identifiers

Primary DI / UDI-DI
27290016923289 EUDAMED
Basic UDI-DI
7290016923AC0005XPX EUDAMED
Direct Marketing DI
27290016923289 EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

IDkit Hp® Two by Meridian Bioscience Israel Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IL-MF-000034713
Authorised Representative
Donawa Lifescience Consulting Srl IT-AR-000007785

Sources (1)

  • EUDAMED bdb4af54-e184-4e49-86c3-9def1d68db26 61 fields · synced Jun 18, 2026