119 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Eu Mdr
×
TELO HP A U 230x260
Device
EU MDR
·
Eu Md Class 1
·PLURITEX SRL·On the market
TELO PERINEO HP A T
Device
EU MDR
·
Eu Md Class 1
·PLURITEX SRL·On the market·3 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market·5 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market·5 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market·5 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market·5 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market·5 countries
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·Not intended for eu market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market
Parafricta
Device
EU MDR
·
Eu Md Class 1
·APA Parafricta Ltd·On the market