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RIDA qLine® Orbital Shaker

EUDAMED

Class A (EU MDR)

Ref ZG2601

by R-Biopharm AG

Identity

Device Name
RIDA qLine® Orbital Shaker EUDAMED
Model / Reference
ZG2601 EUDAMED

Identifiers

Primary DI / UDI-DI
04049095260643 EUDAMED
Basic UDI-DI
4049095ZG26010000PT EUDAMED
EMDN Code
W0201020280 LIMITED PANEL IMMUNOCHEMISTRY ANALYSERS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

RIDA qLine® Orbital Shaker by R-Biopharm AG — Class A — 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 ecde1399-fe35-429d-8d8a-df765c0b38ef 61 fields · synced Jul 24, 2026