8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
A-DEC 2145 DUO UNIT, CUSP
FDA 510(k)
FDA Class 1
·Dental
N/A
FDA UDI
Tyber Medical, LLC·M695M9253200·
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM
RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST
FDA 510(k)
FDA Class 2
·Immunology
WLW
FDA 510(k)
FDA Class 2
·Dental
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·January 22, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 10, 2014