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Neurosign Kartush Disposable Surgical Stimulator +1 more model

FDA UDI

Class II (US FDA UDI)

by The Magstim Company , Ltd.

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 UDI
Elevator 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 +1 more model by The Magstim Company , Ltd. — Class II — FDA UDI — listed in FDA GUDID — 2 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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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