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Rida®unity

EUDAMED

Class A (EU MDR)

Ref ZUNITY

by R-Biopharm AG

Identity

Device Name
RIDA®UNITY EUDAMED
Model / Reference
ZUNITY EUDAMED

Identifiers

Primary DI / UDI-DI
04049095260223 EUDAMED
Basic UDI-DI
4049095ZUNITY0000PA EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS 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

Category: Nucleic acid sample preparation instrument IVD

RIDA UNITY is a cutting-edge medical device designed to detect endocrine disruptors in human tissues. It utilizes advanced spectroscopy technology to analyze biological samples, providing accurate and reliable results. Developed by R-Biopharm AG, this device is ideal for researchers, clinicians, and industries seeking precise measurements.

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

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 b293b50e-058a-41ac-bf50-990a3784bff9 61 fields · synced Jun 28, 2026