← Back to catalogue
Sigma Patient Stimulus Cable
EUDAMEDClass I (EU MDR)
Ref 9438-0173
by Mecta Llc
Identity
- Device Name
- Sigma Patient Stimulus Cable EUDAMED
- Model / Reference
- 9438-0173 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00850037993130 EUDAMED
- Basic UDI-DI
- 00850037993130FZ EUDAMED
- EMDN Code
- Z12109002 ELECTROCONVULSIVE THERAPY (ECT) EQUIPMENT 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
Sigma Patient Stimulus Cable by Mecta Llc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 00850037993130FZ | Class I | No Longer Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mecta Llc
- EUDAMED SRN
- US-MF-000019538
- Authorised Representative
- ICON (LR) Limited IE-AR-000006507
Sources (1)
- EUDAMED f222dfc0-a310-4699-a2b4-d6d9520a8819 61 fields · synced Jul 11, 2026