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Amplidiag Analyzer

EUDAMED

Class IVD General (EU MDR)

Ref AD-ASW

by Mobidiag Ltd.

Identity

Trade Name
Amplidiag Analyzer EUDAMED
Device Name
Amplidiag Analyzer EUDAMED
Model / Reference
AD-ASW EUDAMED

Identifiers

Primary DI / UDI-DI
06430041761204 EUDAMED
Basic UDI-DI
B-06430041761204 EUDAMED
EMDN Code
W02050192 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - IVD MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Special Device Type
-1202 EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Amplidiag Analyzer by Mobidiag Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/IVDD

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Manufacturer

Manufacturer
Mobidiag Ltd.
EUDAMED SRN
FI-MF-000001215

Sources (1)

  • EUDAMED 16052ccf-0799-452f-8639-9e0d5579a300 61 fields · synced Jul 17, 2026