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Amplified Ideia Hp Star Kit

EUDAMED

Class B (EU MDR)

Ref K663011-2

by Oxoid Ltd

Identity

Trade Name
AMPLIFIED IDEIA HP STAR KIT EUDAMED
Device Name
AMPLIFIED IDEIA HP STAR KIT EUDAMED
Model / Reference
K663011-2 EUDAMED

Identifiers

Primary DI / UDI-DI
05032384171811 EUDAMED
Basic UDI-DI
5032384IdeiaHpStarZ6 EUDAMED
EMDN Code
W0105010401 H. PYLORI ANTIGEN DETECTION EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Amplified Ideia Hp Star Kit by Oxoid Ltd — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Oxoid Ltd
EUDAMED SRN
GB-MF-000016914
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (1)

  • EUDAMED 753317b2-5190-4c6f-bee1-24bb0c0f7ff1 61 fields · synced Jun 19, 2026