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Ise Diluent

EUDAMED

Class A (EU MDR)

Ref ISDI-5220

by VitalScientific

Identity

Trade Name
ISE DILUENT EUDAMED
Device Name
ISE DILUENT EUDAMED
Model / Reference
ISDI-5220 EUDAMED

Identifiers

Primary DI / UDI-DI
03701700824213 EUDAMED
Basic UDI-DI
37017008ISDI00AK EUDAMED
EMDN Code
W0101070302 ELECTROLYTE ELECTRODE BUFFERS AND SOLUTIONS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

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

Ise Diluent by Vitalscientific — 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

Manufacturer
VitalScientific
EUDAMED SRN
FR-MF-000004722

Sources (1)

  • EUDAMED 4457af28-786e-4a31-8f28-4060f6d75f83 61 fields · synced May 23, 2026