16 results
·
41ms
·
Sources: EU EUDAMED, US FDA
CardIQ Flow
FDA registration
GE MEDICAL SYSTEMS SCS·2 products·🇫🇷 France
CardIQ Flow
FDA 510(k)
FDA Class 2
·Radiology
SANICURE BV
FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands
CBR ENTERPRISE LIMITED
FDA registration
CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong
BD Veritor System for the Rapid Detection of Flu A+B CLIA Waived kit
FDA registration
BECTON, DICKINSON & CO.·1 product·🇺🇸 United States
NextOrtho6517 (LN) - InterFuse T Intervertebral Body Fusion Device
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
InterFuse T Intervertebral Body Fusion Device
FDA registration
NEXT ORTHOSURGICAL·1 product·🇺🇸 United States
BD Veritor System for the Rapid Detection of Flu A+B CLIA Waived kit
FDA registration
BD Rapid Diagnostics (Suzhou) Co. Ltd.·1 product·🇨🇳 China
BD Veritor System for the Rapid Detection of Flu A+B CLIA Waived kit
FDA registration
BECTON, DICKINSON & CO.·1 product·🇺🇸 United States
invisa-RED ELITE
FDA registration
IR Technology, LLC·1 product·🇺🇸 United States
CREATEC GmbH & CO. KG
FDA registration
CREATEC GmbH & CO. KG·2 products·🇩🇪 Germany
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
BD VERITOR(TM) SYSTEM FOR RAPID DETECTION OF FLU A+B
FDA 510(k)
FDA Class 2
·Microbiology
System, Tomography, Computed, Emission
FDA classification
FDA Class 2
·System, Tomography, Computed, Emission
Devices Detecting Influenza A, B, And C Virus Antigens
FDA classification
FDA Class 2
·Devices Detecting Influenza A, B, And C Virus Antigens
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar