← Back to catalogue

Ideia Lyme Neuroborreliosis Kit

EUDAMED

Class B (EU MDR)

Ref K602811-2

by Oxoid Ltd

Identity

Trade Name
IDEIA LYME NEUROBORRELIOSIS KIT EUDAMED
Device Name
IDEIA LYME NEUROBORRELIOSIS KIT EUDAMED
Model / Reference
K602811-2 EUDAMED

Identifiers

Primary DI / UDI-DI
05032384501854 EUDAMED
Basic UDI-DI
5032384IdeiaLymeUV EUDAMED
EMDN Code
W0105010699 LYME BORRELIOSIS REAGENTS - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

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

Ideia Lyme Neuroborreliosis 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 70960307-a41e-4e90-a6ab-a12e3dc8354d 61 fields · synced Jul 10, 2026