7 results
·
23ms
·
Sources: EU EUDAMED, US FDA
MODIFY ELECTROLYTE ANALYZER MODEL SERA-210
FDA 510(k)
FDA Class 2
·Clinical Chemistry
WI-38
FDA 510(k)
FDA Class 1
·Hematology
FR MEDICAL X-RAY FILM
FDA 510(k)
FDA Class 1
·Radiology
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 3, 2014
ASR ACETABULAR CUPS 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 26, 2012
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 23, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015