17 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL825
FDA 510(k)
FDA Class 2
·General Hospital
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623249·PEEK Corp Core, Ø12x34mm
Brigade
FDA UDI
Nuvasive, Inc.·00887517402288·Brigade Implant, 12x34x28mm 12°
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293111·
TRANSEND EX 14 GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009
ACUNAV DIAGNOSTIC ULTRASOUND CATHETER 8F AND 10F
FDA 510(k)
FDA Class 2
·Cardiovascular
Mistral-Air Warming Unit
FDA 510(k)
FDA Class 2
·Cardiovascular
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
ELECTRIC DERMATOME HANDPIECE
FDA Adverse Event
Malfunction
·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·February 1, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 31, 2014
KAPPA 900 SR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·January 26, 2011
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020