38 results
·
9ms
·
Sources: EU EUDAMED, US FDA
AORTIC OCCLUSION SYSTEMS
Device
EU MDR
·
Eu Md Class 3
·Front Line Medical Technologies Inc.·On the market·12 countries
Spectra Guide Wire Introducer (GWI) Needle
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Spectra Medical Devices, LLC·1 device
Spectra Radio Frequency (RF) Needle
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Spectra Medical Devices, LLC·1 device
MediByte Jr
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·BRAEBON Medical Corporation·1 device
MediByte
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·BRAEBON Medical Corporation·1 device
Transpose Ultra
Basic UDI-DI
EU MDD
·
Eu Md Class 1
·InGeneron Inc.·1 device
Spectra Epidural Needles
Basic UDI-DI
EU MDD
·
Eu Md Class 3
·Spectra Medical Devices, LLC·1 device
Anuform
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Performance Health International LTD·1 device
PERIFORM
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Performance Health International LTD·1 device
Spectra Safe-Cut® Safety Scalpel
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Spectra Medical Devices, LLC·1 device
COBRA-OS Device
Basic UDI-DI
EU MDR
·
Eu Md Class 3
·Front Line Medical Technologies Inc.·1 device
41314634
Certificate
MDD Annex II (excluding section 4)·BRAEBON Medical Corporation·INTERTEK SEMKO AB·1 Basic UDI-DI
41344634
Certificate
MDD Annex II (excluding section 4)·BRAEBON Medical Corporation·INTERTEK SEMKO AB·1 Basic UDI-DI
4130112942
Certificate
MDD Annex V·Performance Health International LTD·INTERTEK SEMKO AB·2 Basic UDI-DIs
41376989-01
Certificate
MDD Annex V·InGeneron Inc.·INTERTEK SEMKO AB·1 Basic UDI-DI
41377776-04
Certificate
MDD Annex II (excluding section 4)·Spectra Medical Devices, LLC·INTERTEK SEMKO AB·4 Basic UDI-DIs
28620163227
Certificate
MDR Technical Documentation·Front Line Medical Technologies Inc.·Intertek Medical Notified Body AB
28620163227
Certificate
MDR Technical Documentation·Front Line Medical Technologies Inc.·Intertek Medical Notified Body AB·1 Basic UDI-DI