7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209135981·
UREA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI
FDA 510(k)
FDA Class 2
·General Hospital
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 9, 2014
CAPSURE SP NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010
ELECTROSURGERY PROBE PLUS II
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·December 3, 2012