9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
CONPHAR UMBILICAL CORD CLAMP
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Catheterization Tray With Bardex® All-Silicone Foley Catheter
FDA UDI
C. R. Bard, Inc.·00801741029660·Catheterization Tray With Bardex® All-Silicone ...
Rongeur
FDA UDI
KATENA PRODUCTS, INC.·00841668108475·KERRISON RONGEUR SIZE 0
Sterile Powder Free Nitrile Examination Glove, Blue Colored, with Non-Pyrogenic Labeling Claim, Sterile Powder Free Nitrile Examination Glove, White Colored, with Non-Pyrogenic Labeling Claim
FDA 510(k)
FDA Class 1
·General Hospital
LIPOEZE LASER ASSISTED ASPIRATION CANNULA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COREVALVE REVALVING SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 16, 2017
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 6, 2014
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·October 15, 2012
CAPSURE SP NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2010