• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
8 records meeting your search criteria returned- Product Code: NEW Product Problem: Device Contaminated During Manufacture or Shipping Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. SFX SYM PDS+ UNI VIO 18IN 1 S/A CTB-1 11/14/2022
ETHICON INC. SFX SYM PDS+ UNI VIO 18IN 0 S/A CT-1 02/02/2022
ETHICON INC. SFX SPI PDS+ UNI VIO 12IN 0 S/A CT-1 01/28/2022
ETHICON INC. PDSII VIO 27IN USP5-0 12/27/2021
ETHICON INC. SFX SYM PDS+ UNI VIO 18IN 0 S/A CT-1 12/17/2021
ETHICON INC. PDSPLUS VIO 8X45 M3 CTB-1 CR::-HOT ROOM 06/14/2021
ETHICON INC. PDSII CLR 18IN 4-0 S/A P-3 PRM MP 05/18/2021
ETHICON INC. PDS PLUS VIO 8X18IN(45CM) USP4-0(M1.5) S 03/30/2021
-
-