| Primary Device ID | 00810007532394 |
| NIH Device Record Key | 4d75ac28-dae5-4270-a9c7-113d739e1a0f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hydrafacial Syndeo |
| Version Model Number | 120V, Black |
| Catalog Number | 7000078-BLK |
| Company DUNS | 364134791 |
| Company Name | Hydrafacial LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| 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 | 00810007532394 [Primary] |
| GFE | Brush, Dermabrasion, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-08-23 |
| Device Publish Date | 2024-07-11 |
| 00810007533711 | 100 –120VAC, 50/60Hz, 2A |
| 00810007533605 | 220-240VAC, 50/60Hz, 2A |
| 00810007532523 | 100–120VAC, 50/60Hz, 2A |
| 00810007532516 | 220-240VAC, 50/60Hz, 2A |
| 00810007532509 | HYDRAFACIAL SYNDEO 120V, WHITE (NO PERK) |
| 00810007532493 | 220-240VAC, 50/60Hz, 2A |
| 00810007532486 | 220-240VAC, 50/60Hz, 2A |
| 00810007532479 | HYDRAFACIAL SYNDEO 120V WHITE |
| 00810007532400 | 220-240VAC, 50/60Hz, 2A |
| 00810007532394 | 100-120VAC, 50/60Hz, 2A |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HYDRAFACIAL SYNDEO 90364837 not registered Live/Pending |
Edge Systems LLC 2020-12-07 |