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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS DMC GMBH COMBI DIAGNOST R90 05/24/2023
PHILIPS MEDICAL SYSTEMS DMC GMBH COMBI DIAGNOST R90 03/08/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA FC 10/29/2022
PHILIPS MEDICAL SYSTEMS DMC GMBH PHILLIPS FLOURO TABLE 09/30/2022
GE MEDICAL SYSTEMS, LLC PRECISION 600 11/19/2019
SIEMENS HEALTHCARE GMBH UROSKOP OMNIA MAX 09/03/2019
SIEMENS AG/SIEMENS HEALTHCARE GMBH UROSKOP OMNIA 03/04/2019
SIEMENS HEALTHCARE GMBH ARTIS Q BIPLANE 01/24/2019
SIEMENS HEALTHCARE GMBH ARTIS Q BIPLANE 01/24/2019
PHILIPS MEDICAL SYSTEMS SYSTEM, X-RAY, FLUOROSCOPIC 10/31/2018
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