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 |