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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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118 records meeting your search criteria returned- Product Code: MFE Product Problem: Entrapment of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
COVIDIEN (IRVINE) ONYX AVM 09/07/2016
MEDTRONIC COVIDIEN ONYX 08/06/2016
MEDTRONIC COVIDIEN ONYX 18 KIT PACKAGED A VM AND TUMOR 07/13/2016
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA ONYX AVM 01/13/2016
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA ONYX 01/06/2016
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA ONYX 12/11/2015
COVIDIEN (IRVINE) ONYX AVM 12/04/2015
COVIDIEN (IRVINE) ONYX AVM 11/26/2015
COVIDIEN (IRIVINE) ONYX 11/04/2015
MEDTRONIC COVIDIEN ONYX KIT 10/07/2015
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