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Polydioxanone Sterilised Surgical Needled Suture - India CDSCO Medical Device Registration

Polydioxanone Sterilised Surgical Needled Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000136_fbbf0f663f145d5bc2b8249e7bad10ad_6ac9bcf04f93f8f76e2d0ab2249cffd4. The license holder is Futura Surgicare Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

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
Polydioxanone Sterilised Surgical Needled Suture
UID: MFG/MD/2020/000136_fbbf0f663f145d5bc2b8249e7bad10ad_6ac9bcf04f93f8f76e2d0ab2249cffd4

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Polydioxanone monofilament synthetic absorbable sutures are indicated for use in all types of soft tissue approximation, including use in pediatric cardiovascular tissue where growth is expected to occur, and ophthalmic surgery. Polydioxanone suture is not indicated in adult cardiovascular tissue, microsurgery and neural tissue. These sutures are particularly useful where the combination of an absorbable suture and extended wound support ##PLACEHOLDER_0## is desirable

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