9 results
·
34ms
·
Sources: EU EUDAMED, US FDA
MS CLASSIQUE BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
SIDUS STEM-FREE SHOULDER, HUMERAL HEAD, 52-23
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWS·March 14, 2019
Ultrasound Scanner System bk2300
FDA 510(k)
FDA Class 2
·Radiology
BLUE ORTHOCORD SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SIDUS STEM-FREE SHOULDER, HEAD DISTRACTOR
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code PKC·October 29, 2019
SARNS
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·June 24, 2014
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 27, 2015
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 21, 2013
SIDUS STEM-FREE SHOULDER, HUMERAL ANCHOR, UNCEMENTED, L
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSD·October 29, 2019