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ELECTROENCEPHALOGRAPH - India CDSCO Medical Device Registration

ELECTROENCEPHALOGRAPH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000905_7696550dec5ba7bc4e05937d2de415cc_60553b9c0f7340dbd4819314d9157741. This device is marketed under the brand name Clarity. The license holder is CLARITY MEDICAL PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
ELECTROENCEPHALOGRAPH
UID: MFG/MD/2023/000905_7696550dec5ba7bc4e05937d2de415cc_60553b9c0f7340dbd4819314d9157741

Brand Name

Clarity

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

EEG can be used in intensive care units for brain function monitoring to monitor for non-convulsive seizures/non-convulsive status epileptics, to monitor the effect of sedative/anesthesia in patients in medically induced coma (Clarity), and to monitor for secondary brain damage in conditions such as sub arachnoids hemorrhaged (Clarity).

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