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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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150 records meeting your search criteria returned- Product Code: LIT Patient Problem: Device Embedded In Tissue or Plaque Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN EVERCROSS 035 08/08/2018
KANEKA CORPORATION SHIRANUI EX 08/07/2018
KANEKA CORPORATION CROSSTELLA RX 08/07/2018
KANEKA CORPORATION CROSSTELLA OTW 08/02/2018
MEDTRONIC MEXICO PACIFIC XTREME 07/31/2018
BOSTON SCIENTIFIC - MAPLE GROVE COYOTE¿ ES 06/14/2018
COVIDIEN FORTREX 0.035 OTW PTA BALLOON CATHETER 06/12/2018
COVIDIEN CHOCOLATE PTA BALLOON CATHETER (OVER THE 05/29/2018
MEDTRONIC MEXICO PACIFIC PLUS 05/14/2018
KANEKA CORPORATION PTA BALLOON CATHETER(OHICHO3) 04/26/2018
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