8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
CMV BIO-BEAD SCREEN KIT
FDA 510(k)
FDA Class 2
·Microbiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517341532·CoRoent® SI Screw, Ø4.5x12mm Self-Drill
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199205·AK3 Congruent Insert Trial Size 6, 12mm
UCP RAPID DRUG SCREENING BUPRENORPHINE, AMP 300, MAMP 500, COC 150 TEST;
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Encision AEM Monopolar Laparoscopic Instruments and Accessories
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014
CAPSUREFIX NOVUS MRI
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 15, 2012
VALIANT CAPTIVIA
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·May 22, 2015