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Magstim Connect

FDA UDI

Class I (US FDA UDI)

by The Magstim Company , Ltd.

Identity

Trade Name
Magstim Connect FDA UDI
Generic Name
Clinical management support software FDA UDI
Model / Reference
5453-00 FDA UDI

Identifiers

Primary DI / UDI-DI
05060229532725 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Clinical management support software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clinical management support software

Magstim Connect by The Magstim Company , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical management support software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca597a67-764a-4f5a-98aa-43e75e881901 33 fields · synced May 29, 2026