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Amp Server Pro 2.1 Software Development Kit

EUDAMED

Class IIa (EU MDR)

Ref 3102008

by Magstim Inc.

Identity

Device Name
Amp Server Pro 2.1 Software Development Kit EUDAMED
Model / Reference
3102008 EUDAMED

Identifiers

Primary DI / UDI-DI
D-3102008UJ EUDAMED
Basic UDI-DI
B-3102008UJ EUDAMED
EMDN Code
Z12100303 SYSTEMS FOR ANALYSING AND MANAGING EEG TRACES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Amp Server Pro 2.1 Software Development Kit by Magstim Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Magstim Inc.
EUDAMED SRN
US-MF-000024844
Authorised Representative
MPS Medical Product Service GmbH DE-AR-000005009

Sources (1)

  • EUDAMED 19e6f905-8afa-44b9-86c2-92e616cd77d4 61 fields · synced Jun 19, 2026