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Neurosign Disposable Twisted Triple Electrodes

FDA UDI

Class II (US FDA UDI)

by The Magstim Company , Ltd.

Identity

Trade Name
Neurosign Disposable Twisted Triple Electrodes FDA UDI
Generic Name
Subdermal needle electrode FDA UDI
Device Name
20mm x 0.3mm needle electrode; 1m cable with TP DIN42802 connector FDA UDI
Model / Reference
1697-00-TE FDA UDI
Description
20mm x 0.3mm needle electrode; 1m cable with TP DIN42802 connector FDA UDI

Identifiers

Primary DI / UDI-DI
05060229530325 FDA UDI
FDA Product Code
IKT FDA UDI
GXZ FDA UDI
GMDN Term
Subdermal needle electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1385 FDA UDI
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 Twisted Triple Electrodes 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

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Manufacturer

Manufacturer
The Magstim Company , Ltd.

Sources (1)

  • FDA UDI dc0cf639-6b43-428a-aee0-a9d2f2b5b92c 36 fields · synced Jun 1, 2026