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ViraSorb

EUDAMED

Class A (EU MDR)

Ref CB002

by Viramed Biotech AG

Identity

Trade Name
ViraSorb EUDAMED
Device Name
Universal Reagent with Cells or Tissues or Derivatives thereof EUDAMED
Model / Reference
CB002 EUDAMED

Identifiers

Primary DI / UDI-DI
EVIRCB0021 EUDAMED
Basic UDI-DI
++EVIRReagentwithCoTQB EUDAMED
Direct Marketing DI
EVIRCB0021 EUDAMED
EMDN Code
W0105900201 BUFFERS (UNASSIGNABLE ), SUPPLEM. REAGENTS, ETC EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

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

ViraSorb by Viramed Biotech 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
Viramed Biotech AG
EUDAMED SRN
DE-MF-000020368

Sources (1)

  • EUDAMED fafbb979-a53c-439c-8b7a-a31482224083 61 fields · synced Sep 18, 2026