| Primary Device ID | 04037691075068 |
| NIH Device Record Key | e035d8d8-5df8-4a88-ab01-3d5ae8514276 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VBT Venous Bubble Trap |
| Version Model Number | BEQ-VBT 160, BIOLINE, Sterile |
| Catalog Number | 70103.0884 |
| Company DUNS | 316153865 |
| Company Name | Maquet Cardiopulmonary AG |
| 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 | true |
| 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 | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com | |
| Phone | +49072229320 |
| info.cp@maquet.com |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 160 Milliliter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04037691075051 [Primary] |
| GS1 | 04037691075068 [Package] Contains: 04037691075051 Package: [8 Units] In Commercial Distribution |
| DTP | Defoamer, cardiopulmonary bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2023-06-02 |
| Device Publish Date | 2017-03-13 |
| 04037691075068 - VBT Venous Bubble Trap | 2023-06-02Venous Bubble Trap, BIOLINE Coating (BEQ), and sterile. The Venous Bubble Trap VBT 160 is designed to remove gross air in the venous line before it is entering the arterial pump and the following components of the extra corporeal circuit (ECC). The VBT has been especially developed as an additional safety feature for minimized systems, e.g. MECC, where venous reservoirs are missing. The VBT is using different physical principals for air removal. |
| 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 |