10,000 results · 49ms · Sources: EU EUDAMED, US FDA

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00812345027457·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00812345027426·Cardiology Information System Workstation

Scribe

FDA UDI
MORTARA INSTRUMENT, INC.·00817655020457·Cardiology Information System Workstation

Scribe

FDA UDI
MORTARA INSTRUMENT, INC.·00817655020587·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022376·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022369·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022437·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022383·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022413·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00812345027433·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00812345027464·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00817655022390·Cardiology Information System Workstation

Modality Manager

FDA UDI
MORTARA INSTRUMENT, INC.·00812345027440·Cardiology Information System Workstation

Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs

FDA 510(k)
FDA Class 1 ·General Hospital

Implanted Phrenic Nerve Stimulator For Central Sleep Apnea

FDA Pre-Market Approval
FDA Class 3 ·remede System

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

FDA Pre-Market Approval
FDA Class 3 ·CERAMAX Ceramic Hip System

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing

FDA Pre-Market Approval
FDA Class 3 ·LCS Total Knee System

System, Test, Her-2/Neu, Nucleic Acid Or Serum

FDA Pre-Market Approval
FDA Class 3 ·PATH VYSION HER-2 DNA PROBE KIT

Fluorescence In Situ Hybridization, Anaplastic Lymphoma Kinase, Gene Rearrangement

FDA Pre-Market Approval
FDA Class 3 ·VYSIS ALK BREAK APART FISH PROBE KIT

ALTHEA

Basic UDI-DI
EU MDR · Eu Md Class 1 ·OFF CARR Srl·12 devices