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Horizon Current Adaptor - Standard
EUDAMEDFDA UDIClass I (EU MDR)
Ref 6601-00Model 3950-00
Identity
- Trade Name
- Horizon Current Adaptor - Standard EUDAMEDFDA UDI
- Generic Name
- Magnetic neural stimulation system FDA UDI
- Device Name
- Double 70mm Placebo Air Film Coil EUDAMEDSham adaptor for HorizonSystems. FDA UDI
- Model / Reference
- 3950-00 EUDAMED6601-00 EUDAMEDFDA UDI
- Description
- Sham adaptor for HorizonSystems. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060229532978 EUDAMEDFDA UDI
- Basic UDI-DI
- 50602295300362 EUDAMED
- Direct Marketing DI
- 05060229532978 EUDAMED
- FDA Product Code
- OBP FDA UDI
- EMDN Code
- Z120606 MAGNETOTHERAPY EQUIPMENT EUDAMED
- GMDN Term
- Magnetic neural stimulation system FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.5805 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Horizon Current Adaptor - Standard by The Magstim Company Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 50602295300362 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- The Magstim Company Limited
- EUDAMED SRN
- GB-MF-000003956
- Authorised Representative
- Technomed Europe NL-AR-000002048
Sources (2)
- EUDAMED 9a545d82-b8be-42fd-91e7-dcaa3e5107d0 61 fields · synced Jul 12, 2026
- FDA UDI 6836541d-f72f-4433-952a-3a550fc6ec05 34 fields · synced May 30, 2026