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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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59 records meeting your search criteria returned- Product Code: GKZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
BECKMAN COULTER UNICEL DXH 900 COULTER CELLULAR ANALYSIS 11/17/2022
BECKMAN COULTER DXH SLIDEMAKER STAINER COULTER CELLULAR 09/20/2022
SYSMEX CORPORATION, I SQUARE SYSMEX XN-20 02/10/2022
ABBOTT LABORATORIES CELL-DYN RUBY SYSTEM 10/21/2021
SYSMEX CORPORATION XT-4000I 05/21/2021
SYSMEX CORPORATION, I SQUARE XN-10 02/16/2021
SYSMEX CORPORATION SYSMEX XN-10 11/30/2020
SYSMEX CORPORATION, I SQUARE XN-10 11/25/2020
SYSMEX CORPORATION, I SQUARE SYSMEX XN-10 10/22/2020
SYSMEX CORPORATION, I SQUARE XN-10 02/24/2020
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