9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
AUTOCATH(TM) SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756379625·GENERAL LAPAROSCOPY PACK
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER 39/+3MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·December 1, 2020
NTI TENSION SUPPRESSION SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
mCare®Powder-free Nitrile Blue Examination Gloves with Chemotherapy Drugs Labeling Claimed
FDA 510(k)
FDA Class 1
·General Hospital
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+3MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·February 16, 2023
ENERGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
MODULAR MICROPLASTY CUP INSERTER
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code LXH·November 30, 2010
ADAPTER SLEEVES 12/14 +2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·July 2, 2014