10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VITRIFREEZE MEDIUM; VITRITHAW MEDIUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Mizzy Comfort Cushion
FDA UDI
Keystone Industries·H66860701351·Scavenger Cap
Vial Adapter
FDA UDI
WEST PHARMA. SERVICES IL, . LTD·07290108240016·Vial Adapter 13mm ML SIL Orange- VF
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108694789·Stepped Depth Pin 2.0/2.4
Cordant
FDA UDI
Seaspine Orthopedics Corporation·10889981115210·35mm
MODELS LYNX AND PANTHER MOTORIZED SCOOTERS, MODELS LYNX SX-3, LYNX SX-3P, LYNX LX-3, LYNX LX-3, PANTHER LX-4
FDA 510(k)
FDA Class 2
·Physical Medicine
PRO.DUCT CATHETER, MODEL CTH03
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 15, 2013
PROVISC (IN DUOVISC)
FDA Adverse Event
Injury
·ALCON - BELGIUM/ S.A. ALCON-COUVREUR N.V.·Product code LZP·April 22, 2011
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEM INC.·Product code JAA·July 9, 2008