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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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7 records meeting your search criteria returned- Product Code: GEA Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN 3ML SMARTIP MED-PREP CANNULA 01/29/2021
CARDINAL HEALTH MONOJECT NEEDLELESS MED PREP CANNULA 03/13/2020
COVIDIEN BLUNT CANNULA 19G X 1 1/2 RP 11/21/2019
CARDINAL HEALTH, INC. MONOJECT 10/10/2019
COVIDIEN 18G BLUNTFILL 01/31/2019
COVIDIEN LP/LLC, DELAND MONOJECT 07/24/2018
DEPUY MITEK CLEAR CANNULA SYSTEM 8.5 X 75 MM ¿ THREA 04/11/2017
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