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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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9 records meeting your search criteria returned- Product Code: IZI Product Problem: Output Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
INTUITIVE SURGICAL, INC ENDOWRIST SP 09/07/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/24/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/23/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/23/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/23/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/23/2023
SIEMENS AG/SIEMENS HEALTHCARE GMBH SIEMENS ARTIS Q BIPLANE 02/06/2023
SIEMENS AG/SIEMENS HEALTHCARE GMBH PROCEDURAL TABLE AXIOM ARTIS Q 03/17/2022
PHILIPS HEALTHCARE ALLURA XPER FD10 10/22/2019
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