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Skin Closure System - India CDSCO Medical Device Registration

Skin Closure System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000182_96c5c889d24183a412babdafc2335034_14ae574bf6eae72a5d6c38f552710fdb. This device is marketed under the brand name CE. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class C. 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 C
Skin Closure System
UID: IMP/MD/2019/000182_96c5c889d24183a412babdafc2335034_14ae574bf6eae72a5d6c38f552710fdb

Brand Name

CE

Device Class

Class C

Approving Authority

CDSCO

Product Information

DERMABONDโ„ข PRINEOโ„ข System is intended for topical application only to hold closed easily approximated skin edges of wounds from surgical incisions including punctures from minimally invasive surgery and simple thoroughly cleansed trauma-induced lacerations. DERMABONDโ„ข PRINEOโ„ข System should be used in conjunction with but not in place of deep dermal stitches. Additionally, the adjunct wound closure device component maintains temporary skin edge alignment along the length of the wound during application of the liquid adhesive.

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