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Neurosign Kartush Disposable Surgical Stimulator - Neurosign Kartush Disposable Surgical Stimulator
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Neurosign Kartush Disposable Surgical Stimulator; Elevator FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- Elevator and 3m extension cable DIN42802 to DIN42802 FDA UDI
- Model / Reference
- 4017-00 FDA UDI
- Description
- Elevator and 3m extension cable DIN42802 to DIN42802 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060229531469 FDA UDI
- FDA Product Code
- ETN FDA UDI
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
- Models / Variants
- Neurosign Kartush Disposable Surgical Stimulator FDA UDIElevator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.1820 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Neurosign Kartush Disposable Surgical Stimulator - Neurosign Kartush Disposable Surgical Stimulator by The Magstim Company , Ltd. — Class II — FDA UDI…
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- The Magstim Company , Ltd.
Sources (1)
- FDA UDI 92dd3bc8-46fa-4061-93d4-b4a76974c430 36 fields · synced May 30, 2026