9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EBI X FIX DYNAFIX SYSTEM (DFS)
FDA 510(k)
FDA Class 2
·Orthopedic
Coulmed
FDA UDI
Coulmed Products Group LLC·10810087350267·Standard Sterile Surgical Gown, Large, AAMI 3
S250-FIT Proton Beam Radiation Therapy Device (S250-FIT)
FDA 510(k)
FDA Class 2
·Radiology
BARRIERPLUS GOLD POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 30, 2015
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 13, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
23GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
25GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020