10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
HEXLOCK/HEXLOCK SCREW
FDA 510(k)
FDA Class 2
·Dental
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123830·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 200mm
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981194673·Interbody, 9mm x 32mm x 16mm, 8 deg
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981202668·Interbody, 9mm x 32mm x 16mm, 8 deg
GORE-TEX DUALMESH EMERGE PLUS BIOMATERIAL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BRONCHOSCOPY ELBOW
FDA 510(k)
FDA Class 2
·Anesthesiology
UNSPECIFIED SAFESET TRANSPAC SETS
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025
HALO360 (230V) GENERATOR
FDA Adverse Event
Injury
·COVIDIEN/BARRX·Product code GEI·January 25, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 17, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 14, 2014