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IMAGE DIAGNOSTICS INC
IMAGE DIAGNOSTICS, INC. · Model 100-4 · UDI-DI 00850977007072
10
510(k) clearances
86
Adverse events
19
Recalls
26
Facilities
Description
IDI,TABLE,VERT.-HORIZ. TABLETOP MOVEMENT,VASCULAR-INTERVENTIONAL-IMAGING,ASPECT 100-4,230V,21IN. WIDE TABLETOP,METRIC ACC'Y RAILS,#A100-2632
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2024-05-31 | Siemens Medical Solutions USA, Inc | Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire |
| 2022-06-02 | GE Healthcare, LLC | As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the ap |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.