Identity
- Trade Name
- Magstim TMS Patient Cap, Size S EUDAMEDMagstim TMS Patient Cap (Size Small) FDA UDI
- Generic Name
- Head marking cap FDA UDI
- Device Name
- Magstim TMS Patient Cap, Size S EUDAMEDThe Magstim TMS Patient Caps are non-sterile medical device accessories, intended to aid in landmark registration during TMS procedures. The user will mark the cap to record various landmarks associated with the treatment or therapy they are conducting. FDA UDI
- Model / Reference
- 5770-00 EUDAMEDFDA UDI
- Description
- The Magstim TMS Patient Caps are non-sterile medical device accessories, intended to aid in landmark registration during TMS procedures. The user will mark the cap to record various landmarks associated with the treatment or therapy they are conducting. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060229532756 EUDAMEDFDA UDI
- Basic UDI-DI
- 50602295300668 EUDAMED
- FDA Product Code
- FYF FDA UDI
- EMDN Code
- N018099 ENCEPHALIC AND PERIPHERAL NERVOUS SYSTEM DEVICES - ACCESSORIES - OTHER EUDAMED
- GMDN Term
- Head marking cap FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4040 FDA UDI
- Market of Registration
- Germany 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
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Magstim TMS Patient Cap, Size S 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 | 50602295300668 | 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 1d71d12a-29dd-4f8b-94ac-047659f44ba1 61 fields · synced Jun 19, 2026
- FDA UDI e4776e62-d797-46e8-a779-a38d0ba90714 34 fields · synced May 30, 2026