| Primary Device ID | 07290016746471 |
| NIH Device Record Key | 513b65c9-cae9-4935-9dad-c41d760ca3ed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | V-VR Handpiece |
| Version Model Number | VTL48010 |
| Catalog Number | VTL48010 |
| Company DUNS | 514612758 |
| Company Name | VIORA LTD |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290016746471 [Primary] |
| PBX | Massager, Vacuum, Radio Frequency Induced Heat |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-09-09 |
| Device Publish Date | 2025-06-03 |
| 07290016746464 - V-ST Single Use tip | 2025-09-09 V-ST Single Use tip |
| 07290016746471 - V-VR Handpiece | 2025-09-09V-VR Handpiece |
| 07290016746471 - V-VR Handpiece | 2025-09-09 V-VR Handpiece |
| 17290016746652 - V-FC Tip | 2025-09-09 V-FC Tip |
| 07290016746785 - V-FC Pro Full | 2025-09-09 Kit of V-FC Pro Handpiece, V-FC Pro Tips and maintenance kit |
| 07290016746808 - V-FC Pro Tip | 2025-09-09 |
| 07290016746815 - V-FC Pro Handpiece | 2025-09-09 |
| 07290016746716 - Console | 2025-07-31 EnerJet Console |
| 07290016746723 - Applicator | 2025-07-31 EnerJet Applicator |