• 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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
137 records meeting your search criteria returned- Product Code: CAI Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST PAUL PORTEX 11/18/2020
ST PAUL GENERAL ANESTHESIA CIRCUITS 11/18/2020
ST PAUL PORTEX GENERAL ANESTHESIA 11/18/2020
ST PAUL GENERAL ANESTHESIA CIRCUITS 11/18/2020
Unknown Manufacturer PORTEX 11/15/2020
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 10/29/2020
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX GENERAL ANESTHESIA CIRCUIT 09/25/2020
VYAIRE MEDICAL 10PK, DUAL,HTD CKT,SPU, PEDPEEPLESS 08/31/2020
INTERSURGICAL UAB BREATHING SYSTEM 08/24/2020
TELEFLEX MEDICAL HUDSON VENTILATOR TUBING SET,LONG LENGTH 07/09/2020
-
-