11 results
·
27ms
·
Sources: EU EUDAMED, US FDA
HSV-2 IGM ELISA TEST
FDA 510(k)
FDA Class 2
·Microbiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756389327·KNEE ARTHROSCOPY PACK
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450210550·
CELL-DYN 4000 IMMUNO T-CELL (CD3/4/8) ASSAY
FDA 510(k)
FDA Class 2
·Hematology
VISENSIA, VISENSIA WITH ALERT
FDA 510(k)
FDA Class 2
·Cardiovascular
REVERSE SHOULDER SYSTEM GLENOSPHERE 39X24.5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·January 12, 2021
SHOULDER SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code PHX·January 16, 2025
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·February 6, 2025
GEMINI SELF-RETAINING CANNULA
FDA Adverse Event
Injury
·FRANTZ MEDICAL DEVELOPMENT, LTD.·Product code NBH·November 23, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 11, 2013
FORTIFY ASSURA DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014