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Flow cell R9 Version

EUDAMED

Class A (EU MDR)

Ref IVD-F-MIN001-RGLModel GridION Dx

by Oxford Nanopore Diagnostics Limited

Identity

Trade Name
Flow cell R9 Version EUDAMED
Model / Reference
GridION Dx EUDAMED
IVD-F-MIN001-RGL EUDAMED

Identifiers

Primary DI / UDI-DI
05056793800124 EUDAMED
Basic UDI-DI
50567938OND-GRD-Dx1-RGLKR EUDAMED
Direct Marketing DI
05056793800124 EUDAMED
EMDN Code
W02050199 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Yes

EUDAMED

New Device

Yes

EUDAMED

Flow cell R9 Version by Oxford Nanopore Diagnostics Limited — Class A — 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

EUDAMED SRN
UK-MF-000046755
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED 45ce4a77-0a14-44ce-b70b-96afb34bef88 61 fields · synced Jul 16, 2026