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L/P Shunts - India CDSCO Medical Device Registration

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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CDSCO Registered
Class Class D
L/P Shunts
UID: IMP/MD/2021/000481_b2eb59cbbf003596f2405bf269567e2a_4e3a9f17bbda8d131bb484c841b27503

Brand Name

CSF-Lumboperitoneal Catheter System

Device Class

Class D

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.

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