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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
 

 
 
8 records meeting your search criteria returned- Product Code: CEM Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
INPECO SA FLEXLAB 03/06/2024
INPECO SA FLEXLAB 10/18/2023
INPECO SA APTIO AUTOMATION 11/23/2022
INPECO SA APTIO AUTOMATION 10/06/2022
INPECO SA APTIO AUTOMATION 05/13/2022
INPECO SA ACCELERATOR A3600 01/12/2022
INPECO SA APTIO AUTOMATION 11/18/2020
INPECO SA APTIO AUTOMATION 12/30/2019
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