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RIDA qLine® SysToBlot

EUDAMED

Class A (EU MDR)

Ref ZG3101CNS

by R-Biopharm AG

Identity

Device Name
RIDA qLine® SysToBlot EUDAMED
Model / Reference
ZG3101CNS EUDAMED

Identifiers

Primary DI / UDI-DI
04049095260278 EUDAMED
04049095260704 EUDAMED
Basic UDI-DI
4049095ZG3101CNS0ZE EUDAMED
EMDN Code
W0201020101 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h) 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® SysToBlot 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 (2)

  • EUDAMED 5b4b9668-166f-4b29-b792-68dd2d72ca54 61 fields · synced Oct 6, 2026
  • EUDAMED f14c5157-8b8f-4897-9c1b-b27f9a217c3b 61 fields · synced May 19, 2026