| Primary Device ID | 00850000712430 |
| NIH Device Record Key | 11b81d03-e285-4dea-a912-144f86634368 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AirSculpt Triple-Port Tubing |
| Version Model Number | AS-8000 |
| Company DUNS | 968286021 |
| Company Name | Millennium Medical Technologies, Inc. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| 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 | 00850000712430 [Primary] |
| GS1 | 00850000712447 [Package] Package: [10 Units] In Commercial Distribution |
| GS1 | 00850000712454 [Package] Contains: 00850000712447 Package: [4 Units] In Commercial Distribution |
| QPB | System, Suction, Lipoplasty For Removal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-12 |
| Device Publish Date | 2025-06-04 |
| 00850000712201 - AirSculpt Console | 2025-06-12 |
| 00850000712379 - AirSculpt Handpiece | 2025-06-12 |
| 00850000712430 - AirSculpt Triple-Port Tubing | 2025-06-12 |
| 00850000712430 - AirSculpt Triple-Port Tubing | 2025-06-12 |
| 00850000712331 - AirSculpt System | 2025-06-11 |
| 00850000712461 - AirSculpt Air Hose (IN) | 2025-06-11 |
| 00850000712423 - Acquicell Pro | 2025-05-02 |
| 00850000712096 - Infiltration Large Bore Tubing | 2023-08-15 |
| 00850000712119 - Disposable Fat Extraction cannula 3.4dis X 20cm | 2023-08-15 |