| Primary Device ID | 06862090171121 |
| NIH Device Record Key | 6e2ac422-8a88-4ade-b65a-fb1e6981bee9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Apilux |
| Version Model Number | SmartPro II |
| Catalog Number | 01-7112 |
| Company DUNS | 246237945 |
| Company Name | Dectro International |
| 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 | 06862090171121 [Primary] |
| 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 | 2 |
| Public Version Date | 2018-07-26 |
| Device Publish Date | 2018-05-22 |
| 06862090171121 | Intense Pulsed Light (IPL) for Treatment of Acne, Vascular Lesions, Pigemented Lesions, Light Ha |
| 06862090171022 | Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal |
| 00686209171125 | Intense Pulsed Light (IPL) for Treatment of Acne, Vascular Lesions, Pigemented Lesions, Light Ha |
| 00686209171026 | Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal |
| 00686209192205 | Intense Pulsed Light unit (IPL) 220Vac |
| 00686209191109 | Intense Pulsed Light unit (IPL) 120Vac |