Primary Device ID | 05060229533005 |
NIH Device Record Key | 653dd7d0-24fe-45ec-bbf4-33b75c57a2c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Horizon 3.0 Interface Unit |
Version Model Number | 5445-00-50 |
Company DUNS | 500375274 |
Company Name | THE MAGSTIM COMPANY LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com | |
Phone | +441994240798 |
regulatory@magstim.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060229533005 [Primary] |
OBP | Transcranial Magnetic Stimulator |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-17 |
Device Publish Date | 2024-05-09 |
05060229532732 | 5790-00 |
05060229533005 | Horizon 3.0 Interface Unit |