15 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LORENZ 1.0MM, 1.5MM, 2.0MM SYSTEM
FDA 510(k)
FDA Class 2
·Dental
1.5MM SYSTEM 4 HOLE LONG STRAIGHT PLATE
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 12, 2017
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221117052·3M™ Victory Series™ First Molar Bands, 953-385,...
I.A.S.S., IV SET W/AIR VENT & I.A.P.S. W/O AIRVENT
FDA 510(k)
FDA Class 2
·General Hospital
BOSTON BRAND HYPOALLERGENIC LATEX GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
D901 LILLIPUT OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·October 13, 2021
CARELINK
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·February 9, 2013
FLEXICAP DISCONNECT CAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·January 8, 2011
ECHELON LINEAR CUTTER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 23, 2014
CUSTOM PERFUSION PACK
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 30, 2012
LILLIPUT 1 START
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·April 17, 2023
LILLIPUT 1 OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALY·Product code DTZ·December 27, 2024
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·December 6, 2024
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·January 17, 2022
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·January 25, 2022