17 results
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110ms
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Sources: EU EUDAMED, US FDA
Innoventa Medica ApS
Manufacturer
🇩🇰 Denmark·3 Basic UDI-DIs·8 Devices·Intertek Medical Notified Body AB, Intertek Medical Notified Body AB, and Intertek Medical Notified Body AB
Box-400 ml SeromaSet (US)
FDA UDI
Innoventa Medica ApS·05700002169785·A sterile container designed to be connected to...
400 ml SeromaSet (US)
FDA UDI
Innoventa Medica ApS·05700002169778·A sterile container designed to be connected to...
GASTROSTOMY, TUBES AND SETS
Device
EU MDR
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Eu Md Class 2b
·Innoventa Medica ApS·On the market·15 countries
GASTROSTOMY, TUBES AND SETS
Device
EU MDR
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Eu Md Class 2b
·Innoventa Medica ApS·On the market·15 countries
Extension tube ENFit 20 cm.
Device
EU MDR
·
Eu Md Class 1
·Innoventa Medica ApS·On the market·10 countries
Extension tube ENFit 30 cm.
Device
EU MDR
·
Eu Md Class 1
·Innoventa Medica ApS·On the market·10 countries
Extension tube ENFit/Luer 27 cm.
Device
EU MDR
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Eu Md Class 1
·Innoventa Medica ApS·On the market·10 countries
Extension tube ENFit 80 cm.
Device
EU MDR
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Eu Md Class 1
·Innoventa Medica ApS·On the market·10 countries
Handset
Device
EU MDR
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Eu Md Class 1
·Innoventa Medica ApS·On the market·8 countries
Extension tube ENFit 15 cm.
Device
EU MDR
·
Eu Md Class 1
·Innoventa Medica ApS·On the market·10 countries
Handset
Basic UDI-DI
EU MDR
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Eu Md Class 1
·Innoventa Medica ApS·1 device
Extension tube ENFit
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Innoventa Medica ApS·5 devices
Lecigon PEG, ENFit
Basic UDI-DI
EU MDR
·
Eu Md Class 2b
·Innoventa Medica ApS·2 devices
68620146168
Certificate
MDR Technical Documentation·Innoventa Medica ApS·Intertek Medical Notified Body AB
28620145188
Certificate
MDR QMS·Innoventa Medica ApS·Intertek Medical Notified Body AB
28620146168
Certificate
MDR Technical Documentation·Innoventa Medica ApS·Intertek Medical Notified Body AB·1 Basic UDI-DI