32 results
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26ms
·
Sources: EU EUDAMED, US FDA
SIGMA
FDA 510(k)
FDA Class 2
·Dental
ETI-CORE-IGMK PLUS
FDA UDI
DIASORIN SPA·08056771102339·
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496001928·MAGIC 70, SIZE M, BLU SCURO, GRADUATED COMPRESS...
SCANLAN® Easy-Tag™ Tracking System
FDA UDI
SCANLAN INTERNATIONAL INC·00846159033007·Easy-Tag Pre-Printed, Broken, Red 250/Spl
NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE
FDA 510(k)
FDA Class 1
·General Hospital
QUINUPRISTIN/DALFOPRISTIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
FDA 510(k)
FDA Class 2
·Microbiology
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·March 30, 2026
DRIVER SHAFT, T-15, LONG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, LONG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
3.0MM HEX DRIVER
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
SMS STEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·March 30, 2026
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·March 11, 2013
PRECISION XTRA
FDA Adverse Event
Injury
·Product code NBW·February 27, 2011
SETROX S 53
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO·Product code DTB·February 15, 2008
Bard PEG Safety System ''Guidewire'' Reorder Number: 001928
FDA Recall
Terminated
·Bard Endoscopic Technologies·Product code FMF·August 4, 2003
UNIVERSAL GLENOID - CENTRAL SCREW 20MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·November 23, 2020