| Primary Device ID | 04033817900283 |
| NIH Device Record Key | b0530812-019a-4485-af21-4c9108ccfc33 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | S5 Roller Pump 150 |
| Version Model Number | Inserts 3/8" x 1/16" |
| Company DUNS | 343225272 |
| Company Name | LivaNova Deutschland GmbH |
| 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 | false |
| Lot Batch | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04033817900283 [Primary] |
| DTQ | CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2024-05-07 |
| Device Publish Date | 2015-10-14 |
| 04033817902713 | RP 150 |
| 04033817900382 | RP 150 |
| 04033817900375 | Inserts Cardioplegia 8:1 |
| 04033817900368 | Inserts Cardioplegia 4:1 |
| 04033817900351 | Inserts Cardioplegia 2:1 |
| 04033817900344 | Inserts Cardioplegia 2:1 |
| 04033817900337 | Inserts Cardioplegia 1:1 |
| 04033817900320 | Inserts Cardioplegia 1:1 |
| 04033817900313 | Inserts 1/2" x 3/32" |
| 04033817900306 | Inserts 1/2" x 1/16" |
| 04033817900290 | Inserts 3/8" x 3/32" |
| 04033817900283 | Inserts 3/8" x 1/16" |
| 04033817900276 | Inserts 1/4" x 3/32" |
| 04033817900269 | Inserts 1/4" x 1/16" |
| 04033817900252 | Inserts 3/16" x 1/16" |
| 04033817900245 | Inserts 1/8" x 1/16" |