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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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275 records meeting your search criteria returned- Product Code: OWB Product Problem: Mechanical Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD20 10/06/2022
SIEMENS HEALTHCARE GMBH ARTIS Q BIPLANE 09/29/2022
SIEMENS HEALTHCARE GMBH ARTIS Q CEILING 08/24/2022
MEDTRONIC NAVIGATION, INC. O-ARM® 07/27/2022
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM O2 IMAGING SYSTEM 07/13/2022
SIEMENS HEALTHCARE GMBH ARTIS ZEE FLOOR 07/06/2022
SIEMENS HEALTHCARE GMBH ARTIS PHENO 06/06/2022
SIEMENS HEALTHCARE GMBH-AT ARTIS Q ZEEGO 04/27/2022
SIEMENS SHENZHEN MAGNETIC RESONANCE LTD. ARTIS ONE 04/22/2022
SIEMENS AG/SIEMENS HEALTHCARE GMBH UROSKOP 04/04/2022
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