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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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14 records meeting your search criteria returned- Product Code: CDD Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BECKMAN COULTER POWER LINK SYSTEM 10/04/2022
CLARE DISCRETE MFG IO ACCESS VITAMIN B12 COBALAMIN 08/02/2021
CLARE DISCRETE MFG IO ACCESS VITAMIN B12 COBALAMIN 08/02/2021
BECKMAN COULTER DYNAMIC INLET, PLC (BULK READY), POWER E 08/29/2019
BREA DISCRETE MFG IO GENERIC CONNECTION UNIT (NCCLS) 08/26/2019
BREA DISCRETE MFG IO POWER PROCESSOR SAMPLE PROCESSING SYSTEM 04/23/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP VB12 ASSAY 12/13/2018
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP VB12 ASSAY 06/29/2018
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP VB12 ASSAY 05/11/2018
SIEMENS HEALTHCARE DIAGNOTICS, INC ADVIA CENTAUR XP VITAMIN B12 (VB12) ASSA 02/14/2018
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