10,000 results · 73ms · Sources: EU EUDAMED, US FDA

BD COR™ GX INSTRUMENT

FDA UDI
BECTON, DICKINSON AND COMPANY·00382904439903·BD COR GX INSTRUMENT

cobas®4800 System Liquid Cytology Preparation Kit

FDA UDI
Roche Molecular Systems, Inc.·00875197003208·

Cervista HTA System

FDA UDI
Hologic, Inc.·15420045501065·

cobas® 4800 System Sample Preparation Kit

FDA UDI
Roche Molecular Systems, Inc.·00875197003178·

BD Onclarity™ HPV Assay

FDA UDI
BECTON, DICKINSON AND COMPANY·00382904419905·BD Onclarity™ HPV Assay Reagent Pack

cobas® 4800 System Wash Buffer Kit

FDA UDI
Roche Molecular Systems, Inc.·00875197003239·

Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

FDA Pre-Market Approval
FDA Class 3 ·CONSULTA CRT-P, SYNCRA CRT-P

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·ADVISA DR

FDA Pre-Market Approval
PROTECTA CRT-D, PROTECTA XT CRT-D

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·REVO MRI SURESCAN

Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

FDA Pre-Market Approval
FDA Class 3 ·ATTAIN ABILITY/ABILITY PLUS/ABILITY STRAIGHT

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·PROTECTA DR/PROTECTA VR/PROTECTA XT DR/PROTECTA XT VR

cobas z 480

FDA UDI
Roche Molecular Systems, Inc.·04015630929016·

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·DIGENE HC2 SYSTEM SOFTWARE

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·cobas HPV Test

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·cobas HPV Test, 240 Tests, cobas HPV Test, 960 Tests

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·DIGENE HYBRID CAPTURE 2 HPV DNA TEST

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·cobas HPV Test

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·BD Onclarity HPV Assay

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval
FDA Class 3 ·HYBRID CAPTURE 2 HIGH-RISK HPV DNA TEST AND HYBRID CAPTURE HPV DNA TEST