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Intra-Abdominal Pressure Monitoring Device

FDA product code PHU · Class U · Unknown

17
Registered devices
114
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-01-13C.R. Bard IncLeaks or disconnect near the sampling port of the Intra Abdominal Pressure Monitoring Device which could lead to the potential of inaccurate readings. The meas

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.