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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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56 records meeting your search criteria returned- Product Code: BSZ Product Problem: Use of Device Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA FABIUS MRI 03/13/2024
DRÄGERWERK AG & CO. KGAA ATLAN A350 02/26/2024
DRÄGERWERK AG & CO. KGAA ATLAN A350 02/08/2024
DRÄGERWERK AG & CO. KGAA ATLAN A350 01/26/2024
DRÄGERWERK AG & CO. KGAA ATLAN A350 01/10/2024
DRÄGERWERK AG & CO. KGAA FABIUS TIRO 11/23/2023
DRÄGERWERK AG & CO. KGAA ATLAN A350 10/17/2023
DRÄGERWERK AG & CO. KGAA FABIUS MRI 10/06/2023
DRÄGERWERK AG & CO. KGAA FABIUS GS 10/05/2023
DRÄGERWERK AG & CO. KGAA FABIUS PLUS 08/28/2023
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