← Back to catalogue

Neurosign Disposable Monopolar Probe, Tapered

FDA UDI

Class II (US FDA UDI)

by The Magstim Company , Ltd.

Identity

Trade Name
Neurosign Disposable Monopolar Probe, Tapered FDA UDI
Generic Name
Nerve-locating system probe, single-use FDA UDI
Device Name
1.5 to 0.5mm tapered electrode 70mm; 1.9m wire with DIN42802 connectors FDA UDI
Model / Reference
3605-00-TE FDA UDI
Description
1.5 to 0.5mm tapered electrode 70mm; 1.9m wire with DIN42802 connectors FDA UDI

Identifiers

Primary DI / UDI-DI
05060229530714 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

Neurosign Disposable Monopolar Probe, Tapered 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c059e287-9ac4-4f3f-a88e-3a40740a8c14 36 fields · synced May 30, 2026