L/P Shunts
- UID
- IMP/MD/2021/000481_b2eb59cbbf003596f2405bf269567e2a_4e3a9f17bbda8d131bb484c841b27503
- Device class
- Class D
- Brand name
- CSF-Lumboperitoneal Catheter System
- Approving authority
- CDSCO
- Product information
- CSF-Lumboperitoneal shunt products are designed for the management of communicating hydrocephalus. They are not appropriate for the treatment of obstructive hydrocephalus unless the patient has had prior surgery establishing a functioning shunt between the cerebral ventricles and the subarachnoid space. Lumboperitoneal shunting is of value in both the diagnosis and treatment of normal pressure (CSF-Lumboperitoneal Catheter System) hydrocephalus. Persistent otorrhea and rhinorrhea may often be satisfactorily controlled by lumboperitoneal shunting. Other indications include hydrocephalus secondary to meningitis and subarachnoid hemorrhage. Lumboperitoneal shunting is also of value in reducing elevated intracranial pressure (CSF-Lumboperitoneal Catheter System), which causes bulging at craniotomy or craniectomy sites, and in the treatment of pseudotumor cerebri.
L/P Shunts is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000481_b2eb59cbbf003596f2405bf269567e2a_4e3a9f17bbda8d131bb484c841b27503. This device is marketed under the brand name CSF-Lumboperitoneal Catheter System. The license holder is India Medtronic Private Limited ,Shed No. 3, Block No. 1, Survey No. 389, 400/2A & 2C, Pudur Main Road, Kuthambakkam - 600124, Poonamallee Taluk, Tiruvallur District ,Tiruvallur Tamil Nadu ,600124 ,India, and it is classified as Device Class Class D. The approving authority is CDSCO.
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