53 results
·
21ms
·
Sources: EU EUDAMED, US FDA
CPAP SYSTEM, MODEL 102001
FDA 510(k)
FDA Class 2
·Anesthesiology
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001318·artVeneer life lower anteriors, UCM, C1
Sonoclot® Reference Plasma Quality Control Kit
FDA UDI
SIENCO, INC.·B55890013181·The Reference Plasma Quality Control Kit is for...
DIAMOND
FDA UDI
SPINAL ELEMENTS·00840916162061·DIAMOND DRILL, 18MM
Rampart One Lumbar Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7401001318·Trial 14mm M 12°
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494462979·Cannulated Femoral Reamer
D 12.0mm, WL 180mm
Phonak Brand
FDA UDI
Sonova AG·07613389399301·myPhonak 4.0 app
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·July 28, 2025
MODIFICATION TO LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET
FDA 510(k)
FDA Class 2
·Immunology
BIONOSTICS GLUCOSE QUALITY CONTROL SOLUTION FOR USE WITH THE FASTTAKE COMPACT BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·March 29, 2022
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·August 19, 2022
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code MEA·August 28, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·March 8, 2023
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·May 31, 2023
8300 ALARIS ETCO2 MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·December 30, 2020
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·January 26, 2023
8300 ALARIS ETCO2 MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·December 21, 2020
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012
8300 ALARIS ETCO2 MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code CCK·December 8, 2020