17 results
·
35ms
·
Sources: EU EUDAMED, US FDA
GCE INTERNATIONAL INC
FDA registration
GCE INTERNATIONAL INC·1 product·🇺🇸 United States
LINDE INTEGRATED VALVE (LIV)
FDA Adverse Event
Malfunction
·Product code ECX·December 31, 2015
PROMETRA INTRATHECAL CATHETER KIT
FDA Adverse Event
Injury
·FLOWONIX MEDICAL, INC.·Product code LKK·November 9, 2018
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·December 17, 2015
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2022
LASERSCAN LSX EXCIMER LASER (CE INTERNATIONAL)
FDA Adverse Event
Injury
·LASERSIGHT TECHNOLOGIES, INC.·Product code LZS·July 5, 2000
CE INTERMATE LV 100, 24 PACK,50126
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·October 18, 2010
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·January 18, 2013
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-REDWOOD CITY·Product code MGB·October 22, 2010
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR -VASCULAR SOLUTIONS·Product code MGB·October 18, 2010
GCP-Service International Ltd. & Co. KG
Authorized representative
🇩🇪 Germany
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices
MDSS GmbH
Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices
Emergo Europe B.V.
Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices
MedNet EC-REP GmbH
Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices
SUNGO Europe B.V.
Authorized representative
🇳🇱 Netherlands·1571 Manufacturers·20390 Devices