18 results
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56ms
·
Sources: EU EUDAMED, US FDA
3CPM Company, Inc.
Manufacturer
🇺🇸 United States·1 Basic UDI-DI·1 Device
3CPM Company., INC.
FDA registration
3CPM Company., INC.·1 product·🇺🇸 United States
3CPM Company, Inc
FDA UDI
3CPM CO., INC.·00864359000223·3CPM Company Electrogastrogram Research/Waterlo...
3CPM Company, Inc
FDA UDI
3CPM CO., INC.·00864359000209·The 3CPM Company, Inc Electrogastrogram Waterlo...
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000247·3CPM EGGSAS Research Interface (Software Only)
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000278·Disposable Electrode and Lead Set for use with ...
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000230·Human Interface Device
3CPM Company, Inc
FDA UDI
3CPM CO., INC.·00864359000216·3CPM Company Electrogastrogram Research platfor...
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000254·Respiratory Belt for 3CPM Electrogastrography s...
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000292·3CPM EGGSAS Research/Waterload Interface (Softw...
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000285·3CPM EGGSAS Waterload Interface (Software Only)
3CPM Company, Inc.
FDA UDI
3CPM CO., INC.·00864359000261·6' leads for use with EGG system
Electrogastrogam(EGG)/Electroviscerogram(EVG)
Device
EU MDR
·
Eu Md Class 2a
·3CPM Company, Inc.·On the market·17 countries
3CPM Electrogastrography/Electroviscerography System
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·3CPM Company, Inc.·1 device
CEpartner4U
Authorized representative
🇳🇱 Netherlands·160 Manufacturers·5787 Devices
OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Product code: H6-25128
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LZO·July 23, 2019
OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code: H6-25328
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LZO·July 23, 2019
OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg hood; Product Code : H5-54840
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LPH·July 23, 2019