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β-Glucan Test R1: Pretreatment Solution

EUDAMED

Class C (EU MDR)

Ref 993-04201Model 993-04201, 997-04101, 995-04401

by FUJIFILM Wako Pure Chemical Corporation

Identity

Trade Name
β-Glucan Test R1: Pretreatment Solution EUDAMED
Device Name
β-Glucan Test R1: Pretreatment Solution, β-Glucan Test R2: LAL Reagent, LAL Control EUDAMED
Model / Reference
993-04201, 997-04101, 995-04401 EUDAMED
993-04201 EUDAMED

Identifiers

Primary DI / UDI-DI
14987481163802 EUDAMED
Basic UDI-DI
498748114987481163802ZB EUDAMED
EMDN Code
W0105060399 MYCOLOGY IMMUNOASSAYS - OTHER EUDAMED
W0105060304 BETA-D-GLUCAN (PAN-FUNGAL MARKERS) EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

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

β-Glucan Test R1: Pretreatment Solution by Fujifilm Wako Pure Chemical Corporation — Class C — 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

EUDAMED SRN
JP-MF-000013944
Authorised Representative
FUJIFILM Wako Chemicals Europe GmbH DE-AR-000011552

Sources (2)

  • EUDAMED b1752cd3-c7c9-47cf-9a93-c1cc9bf62895 61 fields · synced Oct 7, 2026
  • EUDAMED 295f414b-1208-487c-9973-f95cd855c518 61 fields · synced Jul 9, 2026