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RIGHTEST Wiz Plus Blood Glucose Monitoring System

EUDAMEDFDA 510(k)

Class IVD Annex II List B (EU MDR)

Ref 572G01Model GM572510(k) K173139

by Bionime Corporation

Identity

Trade Name
RIGHTEST Wiz Plus Blood Glucose Monitoring System EUDAMED
Device Name
Blood Glucose Monitoring System EUDAMED
Model / Reference
GM572 EUDAMED
572G01 EUDAMED

Identifiers

Primary DI / UDI-DI
D-GM572UN EUDAMED
Basic UDI-DI
B-GM572UN EUDAMED
EMDN Code
W0101060101,W01010699,W0201060102 EUDAMED

Classification

Device Class
Class IVD Annex II List B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

RIGHTEST Wiz Plus Blood Glucose Monitoring System by Bionime Corporation — Class IVD Annex II List B — FDA_510K, IVDD — listed in EUDAMED, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Bionime Corporation
EUDAMED SRN
TW-MF-000008450
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED df44cdfc-f432-49d5-a114-b6c16d3237dc 85 fields · synced Jun 18, 2026
  • FDA 510(k) K173139 1 fields · synced May 18, 2026