← Back to catalogue

AlloSeq cfDNA

EUDAMED

Class IVD General (EU MDR)

Ref ASCF.1(24)-IVD

by CareDx Pty Ltd

Identity

Device Name
AlloSeq cfDNA EUDAMED
Model / Reference
ASCF.1(24)-IVD EUDAMED

Identifiers

Primary DI / UDI-DI
19358706000083 EUDAMED
Basic UDI-DI
B-19358706000083 EUDAMED
EMDN Code
W0106010499 POLYMORPHISM TESTS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

AlloSeq cfDNA by CareDx Pty Ltd — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
CareDx Pty Ltd
EUDAMED SRN
AU-MF-000046711
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 64466261-d896-4ad7-a661-c86a3981b810 61 fields · synced Jul 27, 2026