| Primary Device ID | 20806248005319 |
| NIH Device Record Key | af3ccbd0-9d42-47c2-b836-caf06f98323b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Me |
| Version Model Number | HU-CO00341 |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10806248005312 [Primary] |
| GS1 | 20806248005319 [Package] Contains: 10806248005312 Package: Master carton [2 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 |
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| 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. |