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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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252 records meeting your search criteria returned- Product Code: LWP Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
CPI - DEL CARIBE INGEVITY 06/20/2018
CPI - DEL CARIBE INGEVITY 06/20/2018
CPI - DEL CARIBE INGEVITY 06/20/2018
CPI - DEL CARIBE INGEVITY 06/20/2018
GUIDANT CRM CLONMEL IRELAND ACCOLADE 06/20/2018
GUIDANT CRM CLONMEL IRELAND ALTRUA 06/19/2018
CPI - DEL CARIBE INGEVITY 06/19/2018
CPI - DEL CARIBE INGEVITY 06/19/2018
GUIDANT CRM CLONMEL IRELAND ACCOLADE 05/01/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ASSURITY MRI 04/19/2018
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