Intraluminal Support Device - India CDSCO Medical Device Registration
Intraluminal Support Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000078_ea21d8e78ae044752b24da1104645e60_a4f0020730a4148cb06a14d29d1e013e. This device is marketed under the brand name Flow Re-Direction Endoluminal Device. The license holder is Faith Biotech Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.
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Brand Name
Flow Re-Direction Endoluminal Device
License Holder
Faith Biotech Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
LVIS: [The LVIS device is intended for use with embolic coils for the treatment of intracranial neurovascular diseases.], LVIS Jr.: [The LVIS Jr. device is intended for use with embolic coils for the treatment of intracranial neurovascular diseases.]
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