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Pinnacle Spine Group Disposable XL Monopolar Probe
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Pinnacle Spine Group Disposable XL Monopolar Probe FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- 200mm x 1.5mm electrode; 1.9m wire with DIN42802 connector FDA UDI
- Model / Reference
- 4010-00 FDA UDI
- Description
- 200mm x 1.5mm electrode; 1.9m wire with DIN42802 connector FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060229531353 FDA UDI
- FDA Product Code
- GXZ FDA UDI
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1350 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
Pinnacle Spine Group Disposable XL Monopolar Probe by The Magstim Company , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 db6ea8f0-215b-4a15-bd0b-27720c7a9a84 36 fields · synced Jun 6, 2026