• 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
 

 
 < 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
173 records meeting your search criteria returned- Product Code: CAI Product Problem: Disconnection Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 12/02/2016
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 12/02/2016
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 12/02/2016
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 12/02/2016
CAREFUSION/BD ANES CIRCUIT, ADULT, 108 IN EXP, 2L BAG 11/22/2016
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 11/21/2016
SMITHS MEDICAL ASD, INC. PORTEX® PEDIATRIC DISPOSABLE ANESTHESIA 11/21/2016
CAREFUSION/BD ADULT CIRCUIT (A5U580A4) 11/07/2016
CAREFUSION/BD ANES CIRCUIT, 120 IN EXP, 3L BAG 09/09/2016
CAREFUSION/BD ANES CIRCUIT, ADULT, 124 EXP, 2L BAG 08/19/2016
-
-