| Primary Device ID | 00850000712096 |
| NIH Device Record Key | 04af945b-cf73-4001-88db-e5fa29a08d8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Infiltration Large Bore Tubing |
| Version Model Number | FAT-10002-IN |
| Company DUNS | 968286021 |
| Company Name | Millennium Medical Technologies, Inc. |
| 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 | 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 | 00850000712096 [Primary] |
| KGZ | Accessories, Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-15 |
| Device Publish Date | 2023-08-07 |
| 00850000712201 - AirSculpt Console | 2025-06-12 |
| 00850000712379 - AirSculpt Handpiece | 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 |
| 00850000712096 - Infiltration Large Bore Tubing | 2023-08-15 |
| 00850000712119 - Disposable Fat Extraction cannula 3.4dis X 20cm | 2023-08-15 |