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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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27 records meeting your search criteria returned- Product Code: GKZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ABBOTT LABORATORIES CELL-DYN RUBY SYSTEM 02/13/2024
ABBOTT LABORATORIES CELL-DYN RUBY SYSTEM 12/25/2023
BECKMAN COULTER UNICEL DXH SLIDEMAKER STAINER COULTER CE 10/10/2023
BECKMAN COULTER UNICEL DXH 900 COULTER CELLULAR ANALYSIS 05/10/2023
BECKMAN COULTER UNICEL DXH 800 COULTER CELLULAR ANALYSIS 04/25/2023
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
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