14 results
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45ms
·
Sources: EU EUDAMED, US FDA
FilmArray 2
FDA registration
BioFire Defense, LLC·1 product·🇺🇸 United States
FilmArray 2
FDA registration
BioFire Diagnostics, LLC·1 product·🇺🇸 United States
FilmArray 2.0 System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Instrumentation For Clinical Multiplex Test Systems
FDA classification
FDA Class 2
·Instrumentation For Clinical Multiplex Test Systems
LuxatorLX handpiece
FDA registration
DIRECTA AB·1 product·🇸🇪 Sweden
AD SUPPLY GROUP LIMITED
FDA registration
AD SUPPLY GROUP LIMITED·1 product·🇬🇧 United Kingdom
CBR ENTERPRISE LIMITED
FDA registration
CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong
SANICURE BV
FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands
MAXIM VI KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304205864·
MAXIM® VI KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00887868225932·
GRANTALDER RHAPSODY ACCESS PORT AND CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
STRYKER VENOM ELECTRODES AND CANNULAE
FDA 510(k)
FDA Class 2
·Neurology
Probe, Radiofrequency Lesion
FDA classification
FDA Class 2
·Probe, Radiofrequency Lesion
Port & Catheter, Implanted, Subcutaneous, Intravascular
FDA classification
FDA Class 2
·Port & Catheter, Implanted, Subcutaneous, Intravascular