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Magstim Rapid² Mains Lead Filter 115V

FDA UDI

Class II (US FDA UDI)

by The Magstim Company , Ltd.

Identity

Trade Name
Magstim Rapid² Mains Lead Filter 115V FDA UDI
Generic Name
Magnetic neural stimulation system, stationary FDA UDI
Model / Reference
3801-01 FDA UDI

Identifiers

Primary DI / UDI-DI
05060229532176 FDA UDI
FDA Product Code
GWF FDA UDI
OBP FDA UDI
GMDN Term
Magnetic neural stimulation system, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
882.5805 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Magnetic neural stimulation system, stationary

Magstim Rapid² Mains Lead Filter 115V by The Magstim Company , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic neural stimulation system, stationary.

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 30668661-ffcb-4bd9-8c52-eac8b9f272b6 33 fields · synced May 30, 2026