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Skin Abration Unit - India CDSCO Medical Device Registration

Skin Abration Unit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000817_9e7e37b067011b6d6e94d258f343bd23_7aa95d1364e28005052052c0935a33c5. This device is marketed under the brand name HydraFacial Syndeo System. The license holder is Taevas Life Sciences Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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 B
Skin Abration Unit
UID: IMP/MD/2023/000817_9e7e37b067011b6d6e94d258f343bd23_7aa95d1364e28005052052c0935a33c5

Brand Name

HydraFacial Syndeo System

Device Class

Class B

Approving Authority

CDSCO

Product Information

The System is intended to abrade (HydraFacial Syndeo System) the upper layers of the skin. Indication (related to the use of the device in the European Economic Area (HydraFacial Syndeo System): Mild to moderate acne, i.e., acne vulgaris, comedonal acne (HydraFacial Syndeo System). Superficial acne scarring.

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