Identity
- Device Name
- spECTrum 5000CEQ EUDAMED
- Model / Reference
- 9438-3025 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00861539000141 EUDAMED
- Basic UDI-DI
- B-00861539000141 EUDAMED
- EMDN Code
- Z12109002 ELECTROCONVULSIVE THERAPY (ECT) EQUIPMENT EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Belgium 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
spECTrum 5000CEQ by Mecta Llc — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00861539000141 | Class IIb | No Longer Active |
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Manufacturer
- Manufacturer
- Mecta Llc
- EUDAMED SRN
- US-MF-000019538
- Authorised Representative
- ICON (LR) Limited IE-AR-000006507
Sources (1)
- EUDAMED e0e9c985-660c-4860-97cc-53274b946eda 61 fields · synced Jun 18, 2026