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Saint

FDA UDI

Class II (US FDA UDI)

by Magnus Medical, Inc.

Identity

Trade Name
SAINT FDA UDI
Generic Name
Magnetic neural stimulation system FDA UDI
Device Name
SAINT Neuromodulation System FDA UDI
Model / Reference
SAINT-NMS-1001 FDA UDI
Description
SAINT Neuromodulation System FDA UDI

Identifiers

Primary DI / UDI-DI
00860011072539 FDA UDI
510(k) Number
K220177 FDA UDI
FDA Product Code
OBP FDA UDI
GMDN Term
Magnetic neural stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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
MRI Safety
MR Unsafe FDA UDI

Category: Magnetic neural stimulation system

Saint by Magnus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic neural stimulation system.

Cleared under the same submission

K220177 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Magnus Medical, Inc.

Sources (1)

  • FDA UDI 0b122d70-564e-4916-8302-fd292b031b6e 35 fields · synced May 30, 2026