| Primary Device ID | 17290110121430 |
| NIH Device Record Key | 03946d0e-ffb1-4296-bc30-3785a71a0322 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alma LipoFlow System 50Hz |
| Version Model Number | 1 |
| Catalog Number | AALP24091501 |
| Company DUNS | 532283264 |
| Company Name | ALMA LASERS 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 | 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 | 17290110121430 [Primary] |
| MUU | System, Suction, Lipoplasty |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-08-23 |
| Device Publish Date | 2017-07-25 |
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