Primary Device ID | 20806248006958 |
NIH Device Record Key | 5a55f380-b1b6-4919-855f-5f894e710232 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Me |
Version Model Number | HU-CO00771 |
Company DUNS | 533309022 |
Company Name | ILUMINAGE 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 | 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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10806248006951 [Primary] |
GS1 | 20806248006958 [Package] Contains: 10806248006951 Package: master carton [3 Units] In Commercial Distribution |
ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2016-09-24 |
20806248006958 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248006903 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248006187 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248006071 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248005845 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248005319 | Over-the counter home use device that is intended for the removal of unwanted hair. |
20806248004435 | Over-the counter home use device that is intended for the removal of unwanted hair. |