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 
 > 
 
15 records meeting your search criteria returned- Product Code: JQP Patient Problem: Laceration(s) Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS COBAS P 471 CENTRIFUGE UNIT 01/26/2024
ABBOTT AUTOMATION SOLUTIONS GMBH GLP TRACK END 06/09/2023
BECKMAN COULTER AUTOMATE 2500 12/07/2022
BECKMAN COULTER BIOMEDICAL GMBH RECAPPER 05/17/2022
ROCHE DIAGNOSTICS COBAS 8100 08/03/2021
ROCHE DIAGNOSTICS COBAS 8100 11/04/2020
ROCHE DIAGNOSTICS COBAS P 612 PRE-ANALYTICAL SYSTEM 12/02/2019
ROCHE DIAGNOSTICS COBAS P 512 PRE-ANALYTICAL SYSTEM 08/20/2019
BECKMAN COULTER BIOMEDICAL GMBH AUTOMATE 1250 SAMPLE PROCESSING SYSTEM 08/25/2017
ROCHE DIAGNOSTICS COBAS P 612 PRE-ANALYTICAL SYSTEM 11/08/2016
-
-