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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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96 records meeting your search criteria returned- Product Code: FMF Patient Problem: Device Embedded In Tissue or Plaque Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BD BD PEN NEEDLE 04/07/2014
B. BRAUN MELSUNGEN AG OMNIFIX 03/31/2014
B. BRAUN MELSUNGEN AG OMNIFIX 03/31/2014
BECTON DICKINSON BD PEN NEEDLE 03/24/2014
BECTON DICKINSON BD INSYTE AUTOGUARD 03/24/2014
BD BD ULTRA FINE PEN NEEDLE 01/21/2014
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