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Head Side Pad, 3 Pack

FDA UDI

Class II (US FDA UDI)

by Neuronetics Inc.

Identity

Trade Name
Head Side Pad, 3 Pack FDA UDI
Generic Name
Magnetic neural stimulation system FDA UDI
Device Name
Head Side Pad to be used with the NeuroStar Advanced Therapy System FDA UDI
Model / Reference
81-00848-000 FDA UDI
Description
Head Side Pad to be used with the NeuroStar Advanced Therapy System FDA UDI

Identifiers

Primary DI / UDI-DI
10850005944383 FDA UDI
510(k) Number
K212289 FDA UDI
FDA Product Code
OBP FDA UDI
QCI FDA UDI
GMDN Term
Magnetic neural stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5805 FDA UDI
882.5802 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Magnetic neural stimulation system

Head Side Pad, 3 Pack by Neuronetics 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuronetics Inc.

Sources (1)

  • FDA UDI 40d3daaa-669f-420a-8c97-42b19706fa50 35 fields · synced Jun 8, 2026