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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
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51 records meeting your search criteria returned- Product Code: MDM Product Problem: Device Or Device Fragments Location Unknown Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 06/14/2018
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 05/24/2018
ARTHREX, INC. MULTIFIRE SCORPION 05/21/2018
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 05/17/2018
ARTHREX INC. IBALANCE TKA, FEMORAL SIZER, 0-7 DEG 04/27/2018
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 03/07/2018
ARTHREX INC. SCORPION NEEDLE, HIP LENGTH 02/28/2018
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 10/18/2017
ARTHREX INC. SUREFIRE SCORPION NEEDLE 08/01/2017
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 07/25/2017
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