Mo.Ma Ultra Proximal Cerebral Protection Device
Use the Mo.Ma™ Ultra proximal cerebral protection device to contain and remove all sizes of debris that can dislodge during interventional procedures in the carotid arteries. The Mo.Ma Ultra device with double-occlusion balloon system allows for proximal embolic protection to be established prior to crossing a carotid lesion.
Mo.Ma™ Ultra cerebral protection device is intended to be used during angioplasty and stenting of lesions located in the ICA and/or lesions involving the carotid bifurcation. This device allows protection of the brain from cerebral embolism during the entire duration of the intervention, thus preventing severe and disabling complications. The system allows achieving cerebral protection before target lesion crossing, plus allowing debris removal by blood aspiration at any stage during the procedure.
Mo.Ma Ultra is indicated to be used in patients eligible for carotid angioplasty and/or stenting with stenosis involving the ICA and/or the carotid bifurcation and reference diameter of ECA from 3 to 6 mm and reference diameter of CCA from 5 to 13 mm.
Antegrade flow from the common carotid artery (CCA) and retrograde flow from the external common carotid artery (ECA) are temporarily suspended by dual inflation establishing proximal cerebral protection.
Mo.Ma Ultra Cerebral Proximal Protection Device Animation - (02:23)
View a step-by-step animation of a procedure using the Mo.Ma Ultra proximal cerebral protection device.
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Instructions for Use
Find the technical manual in the product labeling supplied with each device, or by calling technical support for cardiovascular devices: 1-763-526-7890.
|Balloon Material||Compliant elastomeric rubber|
|Balloon Marker Distance‡||6 cm|
|Recommended Guidewire||0.035” (0.89 mm)|
|Balloon Occlusion Range‡||5–13 mm diameter (CCA prox. balloon)
3–6 mm diameter (ECA dist. balloon)
‡Values apply to double-balloon version only.
Minimum Sheath Size (F)
|Inner Diameter of the Working Channel||
See product catalog for complete, detailed product information.
Data on file at Medtronic.
See Instructions for Use for complete procedure requirements.
Values apply to double-balloon version only.