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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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11 records meeting your search criteria returned- Product Code: EZL Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 BARDEX® ALL-SILICONE FOLEY CATHETER 04/06/2022
C.R. BARD, INC. (COVINGTON) -1018233 BARDEX® ALL-SILICONE FOLEY CATHETER 04/06/2022
C.R. BARD, INC. (COVINGTON) -1018233 BARDIA ALL-SILICONE FOLEY CATHETER 01/27/2021
C.R. BARD, INC. (COVINGTON) -1018233 BARDEX LUBRI-SIL I.C. ALL-SILICONE FOLEY 07/29/2020
C.R. BARD, INC. (COVINGTON) -1018233 BARDIA® ALL-SILICONE FOLEY CATHETER 03/20/2020
C.R. BARD, INC. (COVINGTON) -1018233 BARD® SILASTIC® FOLEY CATHETER 03/12/2019
C.R. BARD, INC. (COVINGTON) -1018233 SPECIALTY FOLEYS 07/31/2018
C.R. BARD, INC. (COVINGTON) -1018233 SPECIALTY FOLEYS 07/31/2018
COOK INC UNIVERSA SILICONE FOLEY CATHETER 06/07/2018
C.R. BARD, INC. (COVINGTON) -1018233 BARDEX® ALL-SILICONE TEMPERATURE-SENSING 07/07/2017
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