9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ENZYMUN-TEST PROGESTERONE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756371865·TOTAL HIP PACK
CAPD CATHETER ADAPTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
External Counterpulsation System
FDA 510(k)
FDA Class 2
·Cardiovascular
GMK-SPHERE TIBIAL INSERT - FLEX S3L - 12 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 22, 2020
GMK-SPHERE 02.12.0312FL TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/12 MM L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 8, 2022
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·November 22, 2010
COGNIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LWP·January 11, 2013
PROFEMUR(R) COCR NECK
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code KWA·July 2, 2014