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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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44 records meeting your search criteria returned- Product Code: KZD Product Problem: Leak/Splash Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SUNMED LLC SUNMED LLC 10/11/2023
SALTER LABS SALTER LABS 09/07/2023
SVS LLC PREMIERPRO 03/24/2023
SUNMED HOLDINGS LLC SUNMED LLC 03/10/2023
VYAIRE MEDICAL INC. VITAL SIGNS® PRESSURE INFUSOR 11/10/2022
SMITHS MEDICAL ASD, INC. MEDEX PRESSURE INFUSION C-FUSOR 09/20/2022
SMITHS MEDICAL ASD, INC. MEDEX FDA CLEARED CLEAR-CUFF PRESSURE IN 09/12/2022
SMITHS MEDICAL ASD, INC. MEDEX CLEAR-CUFF PRESSURE INFUSOR 09/10/2022
SMITHS MEDICAL ASD, INC. MEDEX PRESSURE INFUSION C-FUSOR 09/09/2022
SMITHS MEDICAL ASD, INC. MEDEX FDA CLEARED CLEAR-CUFF PRESSURE IN 09/09/2022
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