← Back to catalogue

Glycated Hemoglobin Analyzer

EUDAMED

Class A (EU MDR)

Ref A1c Go

by Goldsite Diagnostics Inc.

Identity

Trade Name
Glycated Hemoglobin Analyzer EUDAMED
Device Name
Glycated Hemoglobin Analyzer EUDAMED
Model / Reference
A1c Go EUDAMED

Identifiers

Primary DI / UDI-DI
06971225930127 EUDAMED
Basic UDI-DI
697122593GS35968AMV EUDAMED
EMDN Code
W0201060101 GLYCOSILATED HEMOGLOBIN DEVICES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

New Device

No

EUDAMED

Glycated Hemoglobin Analyzer by Goldsite Diagnostics Inc. — Class A — 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

EUDAMED SRN
CN-MF-000001353
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 13eba824-76ee-4dc0-b651-751465d8069a 61 fields · synced Jun 18, 2026