9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
CEDIA DAU BARBITURATE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ReLine
FDA UDI
Nuvasive, Inc.·00195377071095·RELINE C Screw, 6.0x30mm MA Thoracic
OMNI Knee
FDA UDI
Omni Life Science, Inc.·00841690101871·Ultra Tibial Insert CS, Size 3 x 10mm
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111154·FOX EYE SHIELD GARTER ASST COLOR PK/50
KLEAR-TEMP
FDA 510(k)
FDA Class 2
·General Hospital
SUCTION TUBES: HOUSE, BARON
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·January 30, 2013
CANALIZER STANDARD ANGLED
FDA Adverse Event
Injury
·PBN MEDICALS DENMARK A/S·Product code DQX·December 9, 2010
IMMERSION HYDROBATH
FDA Adverse Event
Malfunction
·INVACARE CLEVELAND STREET·Product code ILJ·July 15, 2014