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Qtype

EUDAMED

Class C (EU MDR)

Ref 201.701-10Model QTYPE

by CareDx AB

Identity

Device Name
QTYPE EUDAMED
Model / Reference
QTYPE EUDAMED
201.701-10 EUDAMED

Identifiers

Primary DI / UDI-DI
07340035525059 EUDAMED
Basic UDI-DI
73400355QTYPE11TL EUDAMED
Direct Marketing DI
07340035525059 EUDAMED
EMDN Code
W01030403 HLA ANTIGEN TYPING EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Category: HLA class I & II antigen tissue typing IVD, kit, multiplex

Qtype by CareDx AB — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as HLA class I & II antigen tissue typing IVD, kit, multiplex.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
CareDx AB
EUDAMED SRN
SE-MF-000040995

Sources (1)

  • EUDAMED 244b6b5c-db13-4c0e-9380-59a9fa9365da 61 fields · synced Jun 19, 2026