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RIDASCREEN® Adenovirus

EUDAMED

Class B (EU MDR)

Ref C1001K01-VKRef C1001K02-VKRef C1001

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® Adenovirus EUDAMED
Model / Reference
C1001K01-VK EUDAMED
C1001K02-VK EUDAMED
C1001 EUDAMED

Identifiers

Primary DI / UDI-DI
04049095030581 EUDAMED
04049095030598 EUDAMED
04049095030031 EUDAMED
Basic UDI-DI
4049095C100100000FG EUDAMED
EMDN Code
W0105040601 ADENOVIRUS EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

RIDASCREEN® Adenovirus 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 (3)

  • EUDAMED 3f384057-32fe-4675-adba-74a6a7cc2f7a 61 fields · synced Jul 15, 2026
  • EUDAMED 8185010c-1b73-4028-ad29-8a66b6dd59c1 61 fields · synced May 18, 2026
  • EUDAMED e728bb7a-1cec-458e-a1c2-fe3ce3fd15e5 61 fields · synced May 18, 2026