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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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235 records meeting your search criteria returned- Product Code: LNH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS, LLC GE 3.0T SIGNA HDX MR SYSTEM 07/27/2022
SIEMENS HEALTHCARE GMBH - MR MAGNETOM ESPREE SYSTEM 06/28/2022
GE MEDICAL SYSTEMS, LLC. MRI 05/31/2022
SIEMENS HEALTHCARE GMBH - MR MAGNETOM ALTEA 04/28/2022
Unknown Manufacturer 3T MRI 04/21/2022
Unknown Manufacturer MRI 03/25/2022
SIEMENS SHENZHEN MAGNETIC RESONANCE LTD. MAGNETOM SPECTRA 03/25/2022
PHILIPS ELECTRONICS LTD PHILIPS INTERA 1.5T 03/23/2022
Unknown Manufacturer MRI 03/22/2022
RESONANCE TECHNOLOGY, INC. CINEMAVISION GOGGLES 03/21/2022
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