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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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85 records meeting your search criteria returned- Product Code: DRX Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 11/17/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 10/04/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 10/04/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 10/04/2022
NEOTECH PRODUCTS LLC NEOTECH PRODUCTS 09/16/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 04/14/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 04/07/2022
CARDINAL HEALTH 31.1925.21 H92SG ECGELPRSTFOAM57X34MMX50 03/24/2022
CARDINAL HEALTH 100 MEDI-TRACE 100 PK 1000 CA 02/23/2022
MEDICO ELECTRODES INTERNATIONAL LTD NISSHA MEDICAL TECHNOLOGIES 02/04/2022
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