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Maxeeg
EUDAMEDClass I (EU MDR)
Ref DEEG-A (Wire Length: 1.0M Qty: 10PCS)Model DEEG-A-10(10)
Identity
- Trade Name
- MAXEEG EUDAMED
- Device Name
- EEG Cup Electrode EUDAMED
- Model / Reference
- DEEG-A-10(10) EUDAMEDDEEG-A (Wire Length: 1.0M Qty: 10PCS) EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809083943844 EUDAMED
- Basic UDI-DI
- 880908394060KT EUDAMED
- EMDN Code
- N01010202 EEG EXTRACRANIC ELECTRODES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Maxeeg by Bio Protech Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 880908394060KT | Class I | Active |
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Manufacturer
- Manufacturer
- Bio Protech Inc.
- EUDAMED SRN
- KR-MF-000012687
- Authorised Representative
- Meridius Medical Europe Limited IE-AR-000004258
Sources (1)
- EUDAMED d1dbabb0-8603-4620-aec7-8b3c3ab20c4f 61 fields · synced Jul 8, 2026