20 results
·
22ms
·
Sources: EU EUDAMED, US FDA
THERMOPULSE
FDA 510(k)
FDA Class 2
·Physical Medicine
Oticon
FDA UDI
Oticon A/S·05707131259431·NERA, KIT 312 WL DIR 90 R V BE
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365357·Femoral head prosthesis trial - C.F.P. - Hip Stem
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365333·Femoral head prosthesis trial - C.F.P. - Hip Stem
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365340·Femoral head prosthesis trial - C.F.P. - Hip Stem
RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR AND ACCESSORIES (E.G., RITA THERMO PAD AND CABLE ADAPTER)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FORA D40 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LAG SCREWDRIVER GAMMA 3 380 X 110 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code LXH·June 14, 2012
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
ENRHYTHM DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·August 21, 2008
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
MEDISLIM
FDA Adverse Event
Injury
·MEDICREATIONS, LLC·Product code GEX·April 27, 2020
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017