| Primary Device ID | 04037691533339 |
| NIH Device Record Key | 8d8dc664-6b7e-4491-84fd-7e1f8a37555f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | Conv.kit |
| Catalog Number | 70104.7495 |
| Company DUNS | 316153865 |
| Company Name | Maquet Cardiopulmonary AG |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +49072229320 |
| info.cp@maquet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04037691533339 [Primary] |
| KRI | ACCESSORY EQUIPMENT, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-06-30 |
| Device Publish Date | 2015-11-24 |
| 04037691075068 - VBT Venous Bubble Trap | 2023-06-02 Venous Bubble Trap, BIOLINE Coating (BEQ), and sterile. The Venous Bubble Trap VBT 160 is designed to remove gross air in the ve |
| 04037691032528 - NA | 2023-06-02 |
| 04037691576640 - Quadrox-iD | 2022-12-13 |
| 04037691588285 - HLS Set | 2022-12-13 |
| 04037691741130 - NA | 2022-12-08 |
| 04037691741543 - NA | 2022-12-08 |
| 04037691773513 - NA | 2022-12-08 |
| 04037691009025 - NA | 2022-12-06 |