Beckman Coulter Biomedical GmbH
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REM recall (Z-2834-2026) | Beckman Coulter Biomedical GmbH | 2026-07-31 |
| Power Express, REF B90918 recall (Z-2978-2024) | Beckman Coulter Biomedical GmbH | 2024-09-05 |
| PE Centrifuge, REF: B36365, a component of the Power Express recall (Z-2979-2024) | Beckman Coulter Biomedical GmbH | 2024-09-05 |
| PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express. recall (Z-2980-2024) | Beckman Coulter Biomedical GmbH | 2024-09-05 |
| Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, recall (Z-2144-2023) | Beckman Coulter Biomedical GmbH | 2023-07-14 |
| Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60 recall (Z-2145-2023) | Beckman Coulter Biomedical GmbH | 2023-07-14 |
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Every clearance here is in the API, with alerts when new ones post.