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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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11 records meeting your search criteria returned- Product Code: FGB Patient Problem: Bacterial Infection Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
OLYMPUS WINTER & IBE GMBH URETEROSCOPE 09/24/2021
OLYMPUS WINTER & IBE GMBH URETEROSCOPE 09/24/2021
Unknown Manufacturer URETEROSCOPE 04/06/2021
OLYMPUS MEDICAL SYSTEMS CORP. OES URETERORENOFIBERSCOPE 03/11/2021
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 05/21/2019
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 05/20/2019
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 05/20/2019
OLYMPUS MEDICAL SYSTEMS CORP. URETERO-RENO FIBERSCOPE 05/20/2019
OLYMPUS MEDICAL SYSTEMS CORP. FIBERSCOPE "URF-P5", SET E 06/27/2018
KARL STORZ SE & CO. KG URETERO- RENOSCOPE 06/20/2018
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