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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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5 records meeting your search criteria returned- Product Code: DRX Patient Problem: Foreign Body In Patient Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
AMBU A/S AMBU BLUESENSOR R 07/08/2021
LEONHARD LANG GMBH SKINTACT 10/08/2020
AMBU A/S AMBU BLUESENSOR R 10/14/2019
LEONHARD LANG GMBH SKINTACT 07/04/2019
CAREFUSION ELCTD ADT FOAM RND, RDLCNT, SLD GEL 50/P 11/19/2014
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