426 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Eu Mdr
×
DOPPIO CIAK
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
COMBI/P
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CIAK
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R2/APK
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R1/APK
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R2/K
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R1/K
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R4/AP
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R3/AP
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R1/AP
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R2/AP
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R4
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
R3
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/PZ
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/SERV15
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/PZ
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/SERV14
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/SERV5
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/SERV2
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market
CFS/SERV
Device
EU MDR
·
Eu Md Class 1
·CFS ITALIA SRL·On the market