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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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139 records meeting your search criteria returned- Product Code: LNH Product Problem: Use of Device Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE GMBH MAGNETOM AVANTO DOT 11/20/2019
SIEMENS HEALTHCARE GMBH MAGNETOM ESPREE 11/14/2019
GE MEDICAL SYSTEMS, LLC SIGNA PIONEER 11/07/2019
SIEMENS HEALTHCARE GMBH MAGNETOM AERA 10/15/2019
SIEMENS HEALTHCARE GMBH MAGNETOM SKYRA 10/14/2019
GE HEALTHCARE (TIANJIN) COMPANY LIMITED SIGNA EXPLORER 09/17/2019
SIEMENS HEALTHCARE GMBH MAGNETOM ESPREE 09/17/2019
GE MEDICAL SYSTEMS, LLC GE 1.5T SIGNA HDX MR SYSTEM 09/10/2019
GE MEDICAL SYSTEMS, LLC SIGNA PIONEER 09/05/2019
GE MEDICAL SYSTEMS, LLC 3.0T SIGNA HDXT 08/21/2019
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