9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
SECHRIST SERIES 3500 AIR-OXYGEN MIXER
FDA 510(k)
FDA Class 2
·Anesthesiology
ACUMED
FDA UDI
Acumed LLC·10806378094316·5.5/4.3mm Double Drill Sleeve
S40 CREATINE KINASE (CK)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DUAL INCU I
FDA 510(k)
FDA Class 2
·General Hospital
S-ROM M HEAD 36MM +3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 9, 2014
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 23, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 6, 2007
O B TAMPONS SUPER ABSORBENCY
FDA Adverse Event
Malfunction
·MONTREAL SAN PRO·Product code HEB·August 30, 2012
GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
FDA Enforcement
Class II
·Terminated·DePuy Orthopaedics, Inc.·January 19, 2022