7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FOUNTAIN Infusion Catheter and Occluding Guide Wire
FDA 510(k)
FDA Class 2
·Cardiovascular
800 P37,IN,1L,STKR
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828138819·800 P37,IN,1L,STKR
TurboTemp EZ
FDA 510(k)
FDA Class 2
·Dental
ANGLEFIX T LOCKING PLATE, MODELS AF-001 (PLATE), ST-1 (LOCKING SCREW)
FDA 510(k)
FDA Class 2
·Orthopedic
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 6, 2013
ATTAIN ABILITY
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code OJX·February 15, 2011
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 8, 2014