11 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KINETIC AMYLASE DETERMINATION
FDA 510(k)
FDA Class 2
·Clinical Chemistry
GENTLE THREADS TUNNEL DILATOR
FDA UDI
Biomet Orthopedics, LLC·00880304407039·
Gentle Threads™
FDA UDI
Biomet Orthopedics, LLC·00887868568022·
LINER: MPACT FLAT PE HC LINER Ø36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·April 29, 2020
AMI MAMMOSPOT
FDA 510(k)
FDA Class 2
·Radiology
TS-1800 MEDICATION TRANSFER SPIKE
FDA 510(k)
FDA Class 2
·General Hospital
VERSAFITCUP CC TRIO FLAT PE HC LINER 36 / E
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·September 7, 2021
MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 36 SIZE L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·June 8, 2020
COULTER® LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 9, 2013
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 12, 2010
INGENIO
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014