6 results
·
27ms
·
Sources: EU EUDAMED, US FDA
AQUALARM MOISTURE SENSOR MODEL P85000
FDA 510(k)
FDA Class 1
·Anesthesiology
IV BAG PUMP
FDA 510(k)
FDA Class 2
·General Hospital
SPECIFIC IGE EIA-ULTRA ASSAY
FDA 510(k)
FDA Class 2
·Immunology
PROCEDURAL STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·December 10, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·February 6, 2013
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 21, 2014