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PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay

EUDAMED

Class C (EU MDR)

Ref 1500Model PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay

by PentaBase A/S

Identity

Trade Name
PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay EUDAMED
Device Name
PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay EUDAMED
Model / Reference
PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay EUDAMED
1500 EUDAMED

Identifiers

Primary DI / UDI-DI
05713915000410 EUDAMED
Basic UDI-DI
5713915PP004TK EUDAMED
Direct Marketing DI
05713915000410 EUDAMED
EMDN Code
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

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

PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay by PentaBase A/S — Class C — 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
PentaBase A/S
EUDAMED SRN
DK-MF-000023157

Sources (1)

  • EUDAMED 596a0105-2b52-442d-8d73-4fbd3c97167c 61 fields · synced Jun 19, 2026