1,039 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308100·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308080·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308130·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308150·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308140·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308060·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308110·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308120·
Lumbar IBFD
FDA UDI
KEOS·B084KPS12308090·
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Kit, Identification, Neisseria Gonorrhoeae
FDA Pre-Market Approval
FDA Class 1
·GONOSTICON DRI-DOT TEST
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Manual Antimicrobial Susceptibility Test Systems
FDA Pre-Market Approval
FDA Class 2
·UNISCEPT(TM)
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE