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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
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413 records meeting your search criteria returned- Product Code: NIK Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MEDTRONIC EUROPE SARL COBALT¿ XT HF QUAD CRT-D MRI SURESCAN¿ 12/17/2021
MEDTRONIC EUROPE SARL COBALT¿ XT HF QUAD CRT-D MRI SURESCAN¿ 12/10/2021
ABBOTT QUADRA ASSURA MP ICD 12/07/2021
MEDTRONIC EUROPE SARL CLARIA MRI CRT-D SURESCAN 11/17/2021
MEDTRONIC EUROPE SARL CLARIA MRI QUAD CRT-D SURESCAN 11/11/2021
BIOTRONIK SE & CO. KG ITREVIA 7 HF-T DF-1 10/28/2021
BIOTRONIK SE & CO. KG ACTICOR 7 HF-T QP DF4 IS4 PROMRI 10/26/2021
MEDTRONIC EUROPE SARL COBALT HF QUAD CRT-D MRI SURESCAN 10/13/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. CLARIA MRI QUAD CRT-D SURESCAN 10/08/2021
BIOTRONIK SE & CO. KG ITREVIA 7 HF-T QP DF4 IS4 10/07/2021
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