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RIDA qLine® Allergy

EUDAMED

Class B (EU MDR)

Ref A6342PH

by R-Biopharm AG

Identity

Device Name
RIDA qLine® Allergy EUDAMED
Model / Reference
A6342PH EUDAMED

Identifiers

Primary DI / UDI-DI
04049095011238 EUDAMED
Basic UDI-DI
4049095A6X4200000B2 EUDAMED
EMDN Code
W01020204 IMMUNOGLOBULIN E - MONOTEST/PLURIRESULT-MULTI AG EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

RIDA qLine® Allergy by R-Biopharm AG — Class B — 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
R-Biopharm AG
EUDAMED SRN
DE-MF-000007993

Sources (1)

  • EUDAMED 65773107-18e8-4a4d-a2b2-1c09acbcc14c 61 fields · synced Jun 20, 2026