8 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PEDIATRIC ENDOTRACHEAL TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm
Flowflex® Plus Strep A Rapid Test Cassette; Flowflex® Plus Strep A Rapid Test Strip
FDA 510(k)
FDA Class 1
·Microbiology
SELECTIVE-AXIS POSTERIOR NONCERVICAL PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TT (TRACHEOSTOMY TUBES)
FDA Adverse Event
Malfunction
·Product code BTR·October 24, 2017
PULSE-GENERATOR, PACEMAKER, EXTERNAL
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 6, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014