7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
SOLOS EYESITE CANNULAS
FDA 510(k)
FDA Class 1
·Ophthalmic
Lacrimal Probe
FDA UDI
KATENA PRODUCTS, INC.·00841668108826·JACKSON LACRIMAL INTUBATION SET
THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S, THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S, THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALERT A,HDL-APOLIPOROTEIN A, TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·October 12, 2010
SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 13, 2012
LIFEVEST WCD 4000 SYS
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 23, 2014