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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
ABBOTT MANUFACTURING INC ARCHITECT C16000 SYSTEM 06/12/2017
ROCHE DIAGNOSTICS GMBH 8000 C 701 MODULE 04/27/2017
ABBOTT MANUFACTURING INC ARCHITECT I2000SR ANALYZER 03/31/2017
BECKMAN COULTER UNICEL DXC 600 PRO SYNCHRON PRO SYSTEM 03/13/2017
BECKMAN COULTER UNICEL DXC 600I SYNCHRON ACCESS CLINICAL 12/08/2016
BECKMAN COULTER UNICEL DXC 600 PRO SYNCHRON SYSTEM 09/16/2016
BECKMAN COULTER UNICEL DXC 600I SYNCHRON ACCESS CLINICAL 09/16/2016
BECKMAN COULTER UNICEL DXC 600I SYNCHRON ACCESS CLINICAL 09/14/2016
BECKMAN COULTER UNICEL DXC 600I SYNCHRON ACCESS CLINICAL 09/09/2016
BECKMAN COULTER UNICEL DXC 600I SYNCHRON ACCESS CLINICAL 09/09/2016
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