5,451 results
·
45ms
·
Sources: EU EUDAMED, US FDA
Continuous Glucose Monitoring System APP
Basic UDI-DI
EU MDR
·
Eu Md Class 2b
·Changsha Sinocare Inc.·1 device
TouchChat HD w/ WordPower App
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·PRENTKE ROMICH COMPANY·10 devices
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·AudioKey 1.0 and AudioLink
MyBrainCity - The Pain App for YOUths
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·PedScience Vestische Forschungs-gGmbH·1 device
Filtration Stand Electric
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·STRUB GMBH·1 device
pfm medical ag
Authorized representative
🇩🇪 Germany·3 Manufacturers
pfm medical gmbh
Authorized representative
🇩🇪 Germany·3 Manufacturers
GEM Premier 3500
FDA registration
Instrumentation Laboratory Co.·7 products·🇺🇸 United States
GEM Premier 3500
FDA registration
INSTRUMENTATION LABORATORY CO. - Devens·7 products·🇺🇸 United States
GEM Premier 3500
FDA registration
INSTRUMENTATION LABORATORY CO.·7 products·🇺🇸 United States
Anaplasma Spp. And Ehrlichia Spp. Serological Reagents
FDA classification
FDA Not Classified
·Anaplasma Spp. And Ehrlichia Spp. Serological Reagents
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Hybrid L24 Cochlear Implant System
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 22 Cochlear Implant System
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 22 Cochlear Implant System
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 24 Cochlear Implant System
Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 24 Auditory Brainstem Implant System
PUFFClicker3 Inhaler Dose Counter & PUFFClicker3 Companion App
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Aseptika Limited·1 device
3M Deutschland GmbH (Dental)
Importer
🇩🇪 Germany·1 Manufacturer
Sensor, Glucose, Invasive, Non-Adjunctive
FDA Pre-Market Approval
FDA Class 3
·DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
Leishmania Spp. Antigen Detection Assay
FDA classification
FDA Class 1
·Leishmania Spp. Antigen Detection Assay