7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COMPLEMENT ACTIVATION EIA TEST SYSTEM (CAE)
FDA 510(k)
FDA Class 2
·Immunology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm
ABL80 FLEX and ABL80 FLEX CO-OX
FDA 510(k)
FDA Class 2
·Clinical Chemistry
AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE
FDA Adverse Event
Injury
·MPRI·Product code NVN·February 9, 2013
25KHZ PAYNER 360 TIP
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-INAGI·Product code LFL·July 23, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 6, 2011