• 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 
 > 
 
69 records meeting your search criteria returned- Product Code: MCM Product Problem: Failure to Read Input Signal Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COCHLEAR LIMITED NUCLEUS CI622 COCHLEAR IMPLANT WITH SLIM 06/02/2023
OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT 05/16/2023
COCHLEAR LTD NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADV 05/10/2023
COCHLEAR LTD NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADV 05/10/2023
OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT 05/02/2023
OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT 05/02/2023
OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT 05/02/2023
COCHLEAR LTD NUCLEUS CI612 COCHLEAR IMPLANT WITH CONT 05/01/2023
COCHLEAR LIMITED NUCLEUS CI612 COCHLEAR IMPLANT WITH CONT 05/01/2023
OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT 04/28/2023
-
-