10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COMPEX REHAB
FDA 510(k)
FDA Class 2
·Physical Medicine
Amara View
FDA UDI
Respironics, Inc.·00606959009226·Amara View Mask without Headgear, USA, Small
BUTTERFLY PLATE FUNCTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 17, 2024
QUADRA H FEMORAL STEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·July 12, 2012
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NDN·March 14, 2018
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 2, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Death
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 15, 2014
CR TIBIAL INSERT TRIAL #5 - 9MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·April 19, 2011