Healthcare Professionals
Mo.Ma<sup>TM</sup> Ultra Proximal Cerebral Protection Device
Peripheral Interventions
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Healthcare Professionals
Mo.Ma<sup>TM</sup> Ultra Proximal Cerebral Protection Device
Peripheral Interventions
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 internal carotid artery (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™ Double Balloon
Mo.Ma™ Ultra is indicated to be used in patients eligible for carotid angioplasty and/or stenting with stenosis involving the internal carotid artery (ICA) and/or the carotid bifurcation and reference diameter of external carotid artery (ECA) from 3 to 6 mm and reference diameter of common carotid artery (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.
Animation: MoMa Ultra Proximal Cerebral Protection Device - (02:22)
Animation that demonstrates how to use the MoMa Ultra Proximal Cerebral Protection Device to contain and remove all sizes of debris that can dislodge during interventional procedures in the carotid arteries.MoMa, animation, Ultra Proximal Cerebral Protection Device, UC202003387, UC202003387EE
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Instructions for Use
Find this technical manual in the product labeling supplied with each device.
Type | Description |
---|---|
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) |
Reference Number | Minimum Sheath Size (F) | Inner Diameter of the Working Channel |
---|---|---|
MOM0130068X5 |
8 |
0.069"/1.76mm |
MOM0130069X5 |
9 |
0.083"/2.12mm |
See product catalog for complete, detailed product information.
Data on file at Medtronic as per claims matrix UC202115163EN_Claims matrix Mo.Ma Ultra.
See Instructions for Use for complete procedure requirements.