Primary Device ID | 00860011881704 |
NIH Device Record Key | b9ce6fd6-f264-4864-a764-8418d3bf2646 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VSTBalance |
Version Model Number | v2024-01Jan-11-e940.json |
Company DUNS | 117239864 |
Company Name | VIRTUSENSE TECHNOLOGIES, INC. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860011881704 [Primary] |
QKC | Interactive Rehabilitation Exercise Device, Prescription Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-18 |
Device Publish Date | 2024-06-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VSTBALANCE 98842813 not registered Live/Pending |
Virtusense Technologies 2024-11-07 |