Fungus(1-3)-β-D-Glucan Test (Chromogenic Method)

Device name

Fungus(1-3)-β-D-Glucan Test (Chromogenic Method)

Basic UDI-DI

B-06970489560293

Issuing agency

EUDAMED

Version date

May 21, 2026

Applicable legislation

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]

Risk category

IVDD — General

Status

On the market

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

• W01019099Clinical chemistry reagents - other