Primary Device ID | 00860000214018 |
NIH Device Record Key | a9a7c7df-724a-4f1f-aaf1-f004cb38c552 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VPX Vasopulse |
Version Model Number | VPX Vasopulse |
Company DUNS | 109562944 |
Company Name | RESONANT SPECIFIC TECHNOLOGIES, 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 | false |
Serial Number | true |
Manufacturing Date | false |
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 | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com | |
Phone | 866-726-3927 |
info@rstsanexas.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860000214018 [Primary] |
GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2019-04-25 |
00860000214056 - SynRG Light Pad | 2021-09-28 |
00860000214032 - RST-SANEXAS Basic | 2021-04-26 |
00860000214049 - RST-SANEXAS PT | 2021-04-26 |
00860000214025 - SynRG Light Pad | 2019-09-24 |
00860000214001 - neoGEN | 2019-05-23 |
00860000214018 - VPX Vasopulse | 2019-05-23 |
00860000214018 - VPX Vasopulse | 2019-05-23 |