Primary Device ID | 05415067024435 |
NIH Device Record Key | fe434365-f468-419a-9f22-a5d60e7084a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeuroTherm |
Version Model Number | RF-DGP-C |
Catalog Number | RF-DGP-C |
Company DUNS | 124023552 |
Company Name | NEUROTHERM, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Serial Number | false |
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 | +1(855)478-5833 |
customerservice@sjm.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05415067024435 [Primary] |
IKD | CABLE, ELECTRODE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-05-08 |
Device Publish Date | 2016-04-14 |
05415067021564 - Simplicity™ | 2018-11-08 Disposable Radiofrequency Electrode |
15415067021615 - NeuroTherm™ | 2018-11-08 Disposable Radiofrequency Electrode |
15415067022315 - NeuroTherm™ | 2018-11-08 Disposable Radiofrequency Electrode |
05415067026576 - NeuroTherm™ | 2018-11-08 PodiaTherm Disposable Kit |
05415067021243 - NeuroTherm™ | 2018-05-08 |
05415067021250 - NeuroTherm™ | 2018-05-08 |
05415067021298 - NeuroTherm™ | 2018-05-08 |
05415067021328 - NeuroTherm™ | 2018-05-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEUROTHERM 76063816 2575296 Live/Registered |
NEUROTHERM INC. 2000-06-06 |