6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Q-FIX SUTURE ANCHOR, 1.8MM; Q-FIX SUTURE ANCHOR, 2.8MM; DRILL, DRILL GUIDE AND OBTURATOR, 1.8MM & 2.8MM, FIRSTPASS SUTU
FDA 510(k)
FDA Class 2
·Orthopedic
SHENZHEN MED-LINK PULSE OXIMETER PROBE
FDA 510(k)
FDA Class 2
·Cardiovascular
NICHOLS ADVANTAGE BIO-INTACT PTH (1-84) IMMUNOASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·May 29, 2013
JOURNEY BCS
FDA Adverse Event
Injury
·SMTIH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·June 20, 2011
GE OEC 6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 20, 2008