205 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Eu Mdr
×
Myobrace P-3N
Device
EU MDR
·
Eu Md Class 1
·Myofunctional Research Co.·On the market·1 country
Myobrace P-3N
Device
EU MDR
·
Eu Md Class 1
·Myofunctional Research Co.·On the market·1 country
Myobrace P-3N
Device
EU MDR
·
Eu Md Class 1
·Myofunctional Research Co.·On the market·1 country
A-SN/V/799/SFR/22/R
Device
EU MDR
·
Eu Md Class 2a
·Serumwerk Bernburg AG·On the market·5 countries
The Breather Pink
Device
EU MDR
·
Eu Md Class 1
·PN Medical Inc·On the market·4 countries
Breather Recover
Device
EU MDR
·
Eu Md Class 1
·PN Medical Inc·On the market·4 countries
The Breather
Device
EU MDR
·
Eu Md Class 1
·PN Medical Inc·On the market·4 countries
Curafit
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Curafit
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Curafit
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Curafit
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Prokudent
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market
Vitalis
Device
EU MDR
·
Eu Md Class 1
·PS Product Services GmbH·On the market