| Primary Device ID | 00860003838112 |
| NIH Device Record Key | 02c905ab-9882-4c21-a7e3-1f6ddf0f1cd9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Rejuvapen |
| Version Model Number | NXT Model 102 |
| Company DUNS | 012101731 |
| Company Name | Refine Usa, LLC |
| 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 | true |
| 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 | 00860003838112 [Primary] |
| QAI | Powered Microneedle Device |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-28 |
| Device Publish Date | 2023-07-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REJUVAPEN 85841005 4512198 Live/Registered |
Refine USA, LLC 2013-02-05 |