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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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162 records meeting your search criteria returned- Product Code: DXC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MEDTRONIC, INC. TRACELET¿ 05/08/2018
TERUMO CORPORATION, ASHITAKA TR BAND 05/07/2018
ST. JUDE MEDICAL PUERTO RICO, INC. FEMOSTOP¿ GOLD 01/30/2018
ST. JUDE MEDICAL PUERTO RICO, INC. FEMOSTOP¿ GOLD 01/30/2018
ST. JUDE MEDICAL PUERTO RICO, INC. FEMOSTOP¿ GOLD 01/05/2018
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., L VASC BAND 11/06/2017
LEPU MEDICAL TECHNOLOGY LTD. VASC BAND 09/20/2017
MERIT MEDICAL SYSTEMS, INC. MERIT PRELUDE SYNC RADIAL COMPRESSION BA 08/17/2017
TERUMO MEDICAL CORPORATION TR BAND 06/26/2017
MAQUET CV HS III PROXIMAL SEAL 04/12/2017
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