13 results
·
23ms
·
Sources: EU EUDAMED, US FDA
TRAUMA TABLE II
FDA 510(k)
FDA Class 2
·Radiology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867362352·Guidewire, 1.4mm, 3.5mm Beveled FT
COULTER COUNTER MODEL T-660
FDA 510(k)
FDA Class 2
·Hematology
ADD-1
FDA 510(k)
FDA Class 1
·Clinical Chemistry
GUIDEWIRE, 1.6X150MM, CAPITAL FRAG
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code LXH·May 10, 2023
GUIDEWIRE, 1.4MM, 3.5MM BEVELED FT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code LXH·May 10, 2023
CYTO ADMIN 4 LINE SET C110
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·January 22, 2020
JUVEDERM (VOLUME/CONCENTRATION UNK)
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·May 29, 2014
COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 19, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 14, 2012
DRIVER, T10 HEXALOBE, BEVELED FT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 20, 2026
3.5X50MM BEVELED FT SCREW
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·March 20, 2026
CYTO ADMIN 4 LINE SET C110
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·January 14, 2020