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Regional Anaesthesia - India CDSCO Medical Device Registration

Regional Anaesthesia is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000148_aa734f7c6bdfc0f29d1c39644ed5f0f0_b1e65123bb2df1fcc6f8f4f2a7dde5dd. This device is marketed under the brand name Dermafilm & Dermincise. The license holder is VYGON INDIA 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
Regional Anaesthesia
UID: IMP/MD/2019/000148_aa734f7c6bdfc0f29d1c39644ed5f0f0_b1e65123bb2df1fcc6f8f4f2a7dde5dd

Brand Name

Dermafilm & Dermincise

Device Class

Class B

Approving Authority

CDSCO

Product Information

Catheter for continuous plexus blocks and peripheral nerve blocks mainly used for post-operative analgesia after joint surgery

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