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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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138 records meeting your search criteria returned- Product Code: NIK Product Problem: Failure to Disconnect Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUARTET 11/20/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA MP ICD 08/20/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUARTET LEAD SMALL-S, 86 CM 11/27/2018
BIOTRONIK SE & CO. KG LUMAX 540 HF-T 04/05/2018
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) IMPLANTABLE CARDIOVERTER DEFIBRILLATOR 11/21/2016
BIOTRONIK SE & CO. KG ILESTO 7 HF-T DF-1 11/21/2014
BIOTRONIK SE & CO. KG IFORIA 5 HF-T PROMRI DF-1 06/11/2014
ST. JUDE MEDICAL, INC., CRMD ATLAS PLUS HF CRT-D 02/19/2014
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