| Primary Device ID | 00810050860963 |
| NIH Device Record Key | 4111a6b5-c738-4e95-9ee1-763e17199222 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Suction Canister Kit |
| Version Model Number | 100-4145-01 |
| Company DUNS | 556196210 |
| Company Name | LIFEPORT, 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 | false |
| 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 | 00810050860963 [Primary] |
| KDQ | Bottle, Collection, Vacuum |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-05 |
| Device Publish Date | 2021-03-26 |
| 00810050860963 | ASSEMBLY - BRACKET - VAC CANNISTER |
| 00810050860994 | SUCTION CANISTER KIT |
| 00810050862233 | SUCTION CANISTER KIT, DISS, W/O BRACKET, W/LINER, W/ HANDLE |