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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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20 records meeting your search criteria returned- Product Code: BSZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA PERSEUS A500 04/29/2021
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 04/29/2021
MAQUET CRITICAL CARE AB FLOW-I 06/17/2020
MAQUET CRITICAL CARE AB FLOW-I 06/17/2020
DRÄGERWERK AG & CO. KGAA APOLLO 05/14/2020
DRÄGERWERK AG & CO. KGAA FABIUS GS 10/18/2019
DRÄGERWERK AG & CO. KGAA PRIMUS IE 01/21/2019
DRÄGERWERK AG & CO. KGAA FABIUS PLUS 12/20/2018
DRÄGERWERK AG & CO. KGAA PERSEUS A500 12/17/2018
DRÄGERWERK AG & CO. KGAA PRIMUS 11/30/2018
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