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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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7 records meeting your search criteria returned- Product Code: FEO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
GYRUS ACMI, INC. SHOCKPULSE-SE LITHOTRIPSY SYSTEM 08/03/2023
GYRUS ACMI, INC. SHOCKPULSE LITHOTRIPSY PROBE, REUSABLE, 01/10/2023
GYRUS ACMI, INC SHOCKPULSE-SE LITHOTRIPSY SYSTEM 12/17/2021
GYRUS ACMI, INC SHOCKPULSE PROBE SINGLE USE, 3.76MM 3/BX 12/03/2021
GYRUS ACMI, INC SHOCKPULSE-SE LITHOTRIPSY SYSTEM 11/30/2021
GYRUS ACMI, INC SHOCKPULSE-SE LITHOTRIPSY SYSTEM 11/30/2021
GYRUS ACMI INC SHOCKPULSE LITHOTRIPSY TRANSDUCER. 08/11/2020
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