• 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 
 > 
 
66 records meeting your search criteria returned- Product Code: HIH Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GYRUS ACMI, INC CUTTING LOOP (12/PK) 04/18/2019
GYRUS ACMI, INC USA ELITE CF RESECTOSCOPE INNER SHEATH, 04/10/2019
GYRUS ACMI, INC USA ELITE CF RESECTOSCOPE INNER SHEATH, 04/10/2019
GYRUS ACMI, INC USA ELITE CF RESECTOSCOPE INNER SHEATH, 04/10/2019
OLYMPUS WINTER & IBE GMBH INNER SHEATH, FOR 26 FR. OUTER SHEATH, W 03/28/2019
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 24 FR. 03/08/2019
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 24 FR. 02/28/2019
GYRUS ACMI, INC CF RESECTOSCOPE INNER SHEATH, 25FR 02/28/2019
HOLOGIC INC MYOSURE NOVA 02/21/2019
OLYMPUS MEDICAL SYSTEMS CORP. OES HYSTEROFIBERSCOPE 02/18/2019
-
-