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StimGuide Pro MT Coil Tracker Tool
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref 5967-01
Identity
- Trade Name
- StimGuide Pro MT Coil Tracker Tool EUDAMEDFDA UDI
- Generic Name
- Magnetic neural stimulation system FDA UDI
- Device Name
- Repetitive Pulse Magnetic Stimulator Systems (Horizon Family Systems) EUDAMEDStimGuide Pro MT Coil Tracker Tool FDA UDI
- Model / Reference
- 5967-01 EUDAMEDFDA UDI
- Description
- StimGuide Pro MT Coil Tracker Tool FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060229532947 EUDAMEDFDA UDI
- Basic UDI-DI
- 5060229530115Z EUDAMED
- FDA Product Code
- OBP FDA UDI
- EMDN Code
- Z12101105 MAGNETIC STIMULATORS EUDAMED
- GMDN Term
- Magnetic neural stimulation system FDA UDI
Classification
- Device Class
- Class IIb 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
StimGuide Pro MT Coil Tracker Tool by The Magstim Company Limited — Class IIb — 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 | 5060229530115Z | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | 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 0a1afac5-afde-41e1-8ca2-79e7d2ef3f96 61 fields · synced Jul 9, 2026
- FDA UDI 9689b1c2-d934-455b-a836-cb61693969cf 34 fields · synced May 29, 2026