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

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 M3-GOLD AUTOCLAVABLE FOROBLIQUE TELESCOP 04/14/2020
GYRUS ACMI, INC CF RESECTOSCOPE INNER SHEATH, 27FR 04/13/2020
COVIDIEN TRUCLEAR 04/01/2020
HOLOGIC, INC. MYOSURE TISSUE REMOVAL DEVICE 03/25/2020
UNKNOWN GRASPER 03/06/2020
HOLOGIC, INC MYOSURE REACH HYSTEROSCOPIC TISSUE REMOV 03/03/2020
GYRUS ACMI, INC CF RESECTOSCOPE INNER SHEATH, 25FR 02/28/2020
COVIDIEN TRUCLEAR 02/14/2020
OLYMPUS WINTER & IBE GMBH INNER SHEATH, FOR 26 FR. OUTER SHEATH 02/12/2020
OLYMPUS WINTER & IBE GMBH INNER SHEATH, FOR 26 FR. OUTER SHEATH 01/23/2020
-
-