Home › Device types › DPT
Probe, Blood-Flow, Extravascular
FDA product code DPT · Class 2 · Cardiovascular
209
Registered devices
398
Adverse events
24
Recalls
48
510(k) clearances
Devices with this code
Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.BIO-PROBE® — MEDTRONIC, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Bio-Probe® — MEDTRONIC, INC.Moor Instruments Ltd — MOOR INSTRUMENTS LIMITEDMedex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.Moor Instruments Ltd — MOOR INSTRUMENTS LIMITEDMedex — ICU MEDICAL, INC.moorFLPI2- Measurement PC Software — MOOR INSTRUMENTS LIMITEDMedex — ICU MEDICAL, INC.Medex — ICU MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
| 2024-09-24 | Smiths Medical ASD, Inc. | Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
