| Primary Device ID | 06971008271119 |
| NIH Device Record Key | 5bfc5258-3e20-4bb2-a447-8fb59cc0bfc1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Intense Pulsed Light (IPL) System |
| Version Model Number | T023C |
| Company DUNS | 417663470 |
| Company Name | Shenzhen Fansizhe Science And Technology Co., 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 | true |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06971008271119 [Primary] |
| OHT | Light Based Over-The-Counter Hair Removal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-24 |
| Device Publish Date | 2023-04-14 |
| 06971008271065 | T015K |
| 06971008271058 | T015C |
| 06971008271041 | T013C |
| 06971008271034 | T012C |
| 06971008271072 | T015A |
| 06971008271218 | T016K |
| 06971008271201 | T011C |
| 06971008271195 | T001N |
| 06971008271188 | T001B |
| 06971008271171 | T001M |
| 06971008271164 | T001A |
| 06971008271157 | T021A |
| 06971008271140 | T021K |
| 06971008271133 | T023E |
| 06971008271126 | T023D |
| 06971008271119 | T023C |
| 06971008271102 | T023B |
| 06971008271096 | T023A |
| 06971008271089 | T023K |
| 06971008271249 | T033KW |
| 06971008271232 | T002BW |
| 06971008271225 | T002AW |
| 06971008271263 | T033MW |