40 results
·
22ms
·
Sources: EU EUDAMED, US FDA
LASER PREALBUMIN TEST
FDA 510(k)
FDA Class 1
·Immunology
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981125035·20x15x12mm, 15 Degree, Interbody
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·00889981125038·20x15x12mm, 15 Degree, Interbody
Endo-Model SL Knee Prosthesis System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575372331·Femoral Segment, lateral, cemented
AIR-FLOW handy 3.0 PLUS
FDA 510(k)
FDA Class 1
·Dental
COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B
FDA 510(k)
FDA Class 2
·Cardiovascular
ZIMMON BILIARY STENT SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 25, 2018
ZIMMON BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 14, 2018
ZIMMON BILIARY STENT SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·January 9, 2019
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 22, 2021
ZIMMON BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·December 11, 2018
OASIS ONE ACTION STENT INTRODUCTION SYSTEM
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·December 11, 2018
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 16, 2018
FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code LPB·June 5, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·November 29, 2012