| Primary Device ID | 20814716020788 |
| NIH Device Record Key | c543900d-b695-4ec1-a060-51f39e857c28 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 6081K |
| Company DUNS | 809254670 |
| Company Name | COASTAL LIFE 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 | 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 | 00814716020784 [Primary] |
| GS1 | 10814716020781 [Package] Contains: 00814716020784 Package: [5 Units] In Commercial Distribution |
| GS1 | 20814716020788 [Package] Contains: 10814716020781 Package: [6 Units] In Commercial Distribution |
| FYD | Apparatus, Exhaust, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
| 10814716020224 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing |
| 10814716020231 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing |
| 10814716020262 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |
| 10814716020279 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |
| 10814716020729 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |
| 10814716020736 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |
| 10814716020743 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |
| 10814716020750 - Surgimedics® | 2024-05-03 Smoke Evacuation Tubing Adapter |