12 results
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48ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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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
Propper short gas-chex EO sterilization indicators, 250 strips per box, Reorder No. 269001, Propper Manufacturing Co., Inc., Long Island City, N.Y. 11101
FDA Recall
Terminated
·Propper Mfg Co Inc·Product code JOJ·February 7, 2008
Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product Description: Common Name: Diagnostic intravascular catheter Description: The Novasight Hybrid catheter is a 3Fr single use, sterile device, which will be able to perform transluminal ultrasound and optical coherence tomography imaging of adults. The catheter is capable of real-time 2D side viewing ultrasound and optical imaging acquired simultaneously providing precisely co-registered images with the ability to produce rapidly post processed rendered longitudinal images of the vessel. Packaging: The Novasight Hybrid Catheter is packaged in a packaging system including the protective packaging and the sterile barrier system.
FDA Recall
Open, Classified
·Conavi Medical Inc.·Product code OBJ·March 12, 2025