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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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66 records meeting your search criteria returned- Product Code: DRE Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CORDIS CASHEL SI AVANTI+ 7F STD W/GW NO OBT 08/09/2019
CORDIS CORPORATION 4F 10CM HW RADIAL 07/29/2019
CORDIS CORPORATION SI AVANTI+ 9F STD W/GW NO OBT 05/06/2019
CORDIS CORPORATION SI AVANTI+ PED .035 F6 W/GW 08/29/2018
CORDIS DE MEXICO SI AVANTI+ .035 F8 W/MINI GW 06/11/2018
MERIT MEDICAL SYSTEMS, INC. HVA - HEMOSTASIS VALVE ADAPTER 02/22/2018
MERIT MEDICAL SYSTEMS, INC. HVA - HEMOSTASIS VALVE ADAPTER 02/22/2018
COOK INC AQ HYDROPHILIC COATED DILATOR 02/19/2018
COOK INC AQ HYDROPHILIC COATED DILATOR 02/19/2018
CORDIS CORPORATION AVANTI + 5F STD W/GW 08/03/2017
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