Identity
- Device Name
- EGI Response Pad 200 EUDAMED
- Model / Reference
- 4608150 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-4608150YJ EUDAMED
- Basic UDI-DI
- B-4608150YJ 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
EGI Response Pad 200 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-4608150YJ | Class IIa | Active |
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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 4fcbe061-1ae7-4be7-91c6-b71138a556e7 61 fields · synced Jul 23, 2026