9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Regenalase Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CoRoent
FDA UDI
Nuvasive, Inc.·00887517570543·CoRoent Ant TLIF Ti, 13x13x34mm 4°
alésoir Ø9
FDA UDI
FOURNITURES HOSPITALIERES INDUSTRIE·03661489333446·
MINICAP HB A1C, MINICAP FLEX-PIERCING, HB A1C CAPILLARYS CONTROLS, HBA1C CAPILLARYS CALIBRATORS
FDA 510(k)
FDA Class 2
·Hematology
LIGAND PLUS CONTROL LEVEL 1-3
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TRAUMAONE SYSTEM DRILL, 1.6X50MM 22MM STOP
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HBE·October 25, 2018
AFX SYSTEM
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·November 6, 2014
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 2, 2011
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2013