• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 3 
 4 
 > 
 
33 records meeting your search criteria returned- Product Code: BYD Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SUNMED HOLDINGS LLC. MEDLINE 08/21/2020
TELEFLEX MEDICAL SDN. BHD. HUSON HUMID-VENT 2S FLEX,STERILE 06/26/2020
TELEFLEX INCORPORATED HUDSON RCI 08/05/2019
VYAIRE MEDICAL HME TYPE I ADULT 05/01/2019
TELEFLEX MEDICAL HUDSON HUMID-VENT 2S FLEX,CLEAN 08/20/2018
TELEFLEX MEDICAL HUDSON HUMID-FLO HME 07/11/2018
TELEFLEX MEDICAL HUDSON HUMID-FLO HME 07/11/2018
AMSINO MEDICAL GROUP HONG KONG CO LTD HME TYPE I ADULT 06/28/2018
AMSINO MEDICAL GROUP HONG KONG CO LTD HME TYPE I ADULT 06/18/2018
AMSINO MEDICAL GROUP HONG KONG CO LTD HME TYPE I ADULT 06/18/2018
-
-