FDA UDI In Commercial Distribution 🇺🇸 United States

NeuroSITE

DI: 00850005944300 · Model: 81-72024-000 · NEURONETICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NeuroSITE
Primary DI
00850005944300
Version / Model
81-72024-000
Company Name
NEURONETICS, INC.
Labeler DUNS
134960348
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-03
Public Version
1
Public Version Date
2024-01-11
Public Version Status
New
Public Device Record Key
e34a04d0-ebae-427e-8393-1f1cb209557f

Device Description

The NeuroSITE is used to aid in the process of determining and recording the coil locations during the motor threshold (MT) and treatment processes.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QCI Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder
OBP Transcranial Magnetic Stimulator

GMDN Terms

Code Name
61124 Magnetic neural stimulation system

Identifiers

Type ID
Package 10850005944307
Primary 00850005944300

Customer Contacts

Phone
877-600-7555

Premarket Submissions

Submission Number Supplement Number
K233621 000