Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
21 records meeting your search criteria returned- Product Code: OSI Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HILL-ROM BATESVILLE CNTROLR, RNT CLRT 120V US 06/27/2024
HILL-ROM BATESVILLE COMPELLA CAP US SCALE PD PPM 06/25/2024
HILL-ROM BATESVILLE COMPELLA CAP US SCALE PD PPM 06/25/2024
XIAMEN WORLD GEAR SPORTS GOODS CO., LTD DRIVE 05/29/2024
XIAMEN WORLD GEAR SPORTS GOODS CO., LTD DRIVE 05/24/2024
HILL-ROM BATESVILLE COMPELLA CAP US SCALE STEER BE 08/23/2023
CAREMED BARIATRIC BED 08/12/2023
XIAMEN WOELD GEAR SPORTS GOODS DRIVE 10/26/2021
JOERNS HEALTHCARE BARI10A BARAIATRIC BED 07/27/2020
JOERNS HEALTHCARE BARI10A BARIATRIC BED 09/10/2019
-
-