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

MAUDE - Manufacturer and User Facility Device Experience
  • 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
 

 
 
5 records meeting your search criteria returned- Product Code: CAI Product Problem: Partial Blockage Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WESTMED LLC WESTMED LLC 03/24/2023
INTERSURGICAL INC. BREATHING CIRCUIT 04/09/2018
VYAIRE MEDICAL, INC ANES CIRCUIT, ADULT, 72 IN CORR, 3L BAG 07/12/2017
CAREFUSION, INC ANES CIRCUIT, ADULT, 108 IN EXP, 3L BAG 11/30/2016
WESTMED, INC. ANESTHESIA CIRCUIT 09/16/2015
-
-