36 results
·
23ms
·
Sources: EU EUDAMED, US FDA
GLOBAL HEALTHCARE VAGINAL SPECULUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519899·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519905·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519936·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519912·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519950·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519929·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033519943·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012979·PedFuse Remind LES, Quad-H, 7.0mm x 35mm
POSI-GRIP UMBILICAL CORD CLAMP, STERILE, MODEL 384, POSI-GRIP UMBILICAL CORD CLAMP, NON-STERILE, MODEL 385
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
JAS MAGNESIUM REAGENT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
HEALONID GV
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 27, 2001
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MPRI·Product code DTB·March 20, 2013
VIBRANT SOUNDBRIDGE
FDA Adverse Event
Malfunction
·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·February 4, 2011
SUMMIT 2.0MM HEX DRIVER SHAFT
FDA Adverse Event
Malfunction
·DEPUY SPINE, INC.·Product code LXH·March 14, 2008
METASUL, ALPHA INSERT, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·March 15, 2018
METASUL, ALPHA INSERT, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·June 25, 2018
DURASUL, ALPHA INSERT, KK/36
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·March 6, 2018
DURASUL, ALPHA INSERT, HOODED, MM/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·May 22, 2018
DURASUL, ALPHA INSERT, HH/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·June 4, 2018