| Primary Device ID | 00810007531540 |
| NIH Device Record Key | 9aaaab3e-de43-4dab-bc3f-da884c99157e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hydrafacial MD Elite |
| Version Model Number | 120V |
| Catalog Number | 70143-03-01 |
| 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 | 00810007531540 [Primary] |
| GFE | Brush, Dermabrasion, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-26 |
| Device Publish Date | 2024-07-18 |
| 00810007531540 | 100–120VAC, 50/60Hz, 8A |
| 00810007531311 | 220-240VAC, 50/60Hz, 8A |