10 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip Catheter
FDA UDI
Unisensor AG·07640172973547·
IMBIBE BONE MARROW ASPIRATION SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
CMAP PRO
FDA 510(k)
FDA Class 2
·Physical Medicine
CRUCIFORM SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HXX·May 10, 2017
DEK BL MF 0 TC-43 2N 48"
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GAW·May 17, 2017
CLEARLINK BURETROL SOLUTION SETS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 13, 2023
COULTER® AC*T DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 21, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 14, 2011