• 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 
 > 
 
71 records meeting your search criteria returned- Product Code: FZP Product Problem: Unintended Ejection Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG CHALLENGER TI-P ML-LIGAT.CLIPS 12 CARTR. 04/07/2023
AESCULAP AG LIGATING CLIPS M/L 12/BOX 03/15/2023
AESCULAP AG CHALLENGER TI-P SM-LIGAT.CLIPS 12 CARTR. 03/08/2023
AESCULAP AG LIGATING CLIPS M/L 12/BOX 02/24/2023
AESCULAP AG CHALLENGER TI-P ML-LIGAT.CLIPS 12 CARTR. 12/28/2022
AESCULAP AG LIGATING CLIPS M/L 12/BOX 12/05/2022
AESCULAP AG CHALLENGER TI-P SM-LIGAT.CLIPS 12 CARTR. 11/29/2022
AESCULAP AG CHALLENGER TI-P ML-LIGAT.CLIPS 12 CARTR. 11/28/2022
AESCULAP AG CHALLENGER TI-P ML-LIGAT.CLIPS 12 CARTR. 08/10/2022
AESCULAP AG CHALLENGER TI-P ML-LIGAT.CLIPS 12 CARTR. 08/10/2022
-
-