| Primary Device ID | 10803622106009 |
| NIH Device Record Key | 844355f4-0e11-4157-96ec-ca3100d27129 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Thoracic Drain |
| Version Model Number | TC-xxxxx |
| Company DUNS | 080914995 |
| Company Name | LIVANOVA USA, 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00803622106002 [Primary] |
| GS1 | 10803622106009 [Package] Contains: 00803622106002 Package: CASE [10 Units] In Commercial Distribution |
| GBS | CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-08-15 |
| Device Publish Date | 2015-07-16 |
| 10803622106078 | TC-xxxxx |
| 10803622106061 | TC-xxxxx |
| 10803622106054 | TC-xxxxx |
| 10803622106047 | TC-xxxxx |
| 10803622106030 | TC-xxxxx |
| 10803622106023 | TC-xxxxx |
| 10803622106016 | TC-xxxxx |
| 10803622106009 | TC-xxxxx |
| 10803622105996 | TC-xxxxx |
| 10803622105989 | TC-xxxxx |
| 10803622105972 | TC-xxxxx |
| 10803622105965 | TC-xxxxx |
| 10803622105958 | TC-xxxxx |
| 10803622105941 | TC-xxxxx |
| 10803622105934 | TC-xxxxx |
| 10803622105927 | TC-xxxxx |