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501rp+

EUDAMED

Class A (EU MDR)

Ref 0023295

by Tosoh Corporation

Identity

Trade Name
501RP+ EUDAMED
Device Name
501RP+ EUDAMED
Model / Reference
0023295 EUDAMED

Identifiers

Primary DI / UDI-DI
04562185402094 EUDAMED
Basic UDI-DI
45601892100040057P EUDAMED
EMDN Code
W020106019082 VARIOUS DIABETES MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED
W0201050292 HIGH PERFORMANCE LIQUID CHROMATOGRAPHY SYSTEMS - IVD MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class A EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Belgium 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

501rp+ by Tosoh Corporation — 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
Tosoh Corporation
EUDAMED SRN
JP-MF-000024143
Authorised Representative
Tosoh Europe N.V. BE-AR-000000211

Sources (2)

  • EUDAMED 0c5f8e08-3581-4749-96aa-28a3046653d2 61 fields · synced Jun 19, 2026
  • EUDAMED 563f3d8a-9f61-4a52-bbe3-ce988383d9c8 61 fields · synced Jun 19, 2026