Maquet Cardiopulmonary Gmbh
2 FDA 510(k) clearances · Recalling firm
◉ Watch Maquet Cardiopulmonary Gmbh
| Record | Firm | Date |
|---|---|---|
| Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720; recall (Z-1300-2026) | Maquet Cardiopulmonary Gmbh | 2026-02-05 |
| Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bag recall (Z-2193-2025) | Maquet Cardiopulmonary Gmbh | 2025-07-29 |
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Every clearance here is in the API, with alerts when new ones post.