8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
N20 TEST
FDA 510(k)
FDA Class 2
·Anesthesiology
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209118663·
AEROLIFE ULTRASONIC NEBULIZER, MODEL P2C
FDA 510(k)
FDA Class 2
·Anesthesiology
ADMIRE
FDA 510(k)
FDA Class 2
·Radiology
EADE RT PM MINI RVS GLENOID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·July 13, 2022
UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·October 5, 2010
SPECTRUM INFUSIOIN PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 23, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 30, 2012