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Vena Cava Filter - India CDSCO Medical Device Registration

Vena Cava Filter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000404_c9bea13a0ae2b7c9e275dac663f86bc3_4244b78d8957d967c545659b507db7ca. This device is marketed under the brand name ASD. The license holder is Lifetech Scientific India Pvt. Ltd., and it is classified as Device Class Class D. 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 D
Vena Cava Filter
UID: IMP/MD/2018/000404_c9bea13a0ae2b7c9e275dac663f86bc3_4244b78d8957d967c545659b507db7ca

Brand Name

ASD

Device Class

Class D

Approving Authority

CDSCO

Product Information

AegisyTM Vena Cava Filter is indicated for filtrating thrombus after percutaneous placement in the inferior vena cava in the following situations: ๏‚Ÿ Pulmonary embolism, when anticoagulants are contraindicated ๏‚Ÿ Failure of anticoagulant therapy in thrombo-embolic diseases ๏‚Ÿ Emergency treatment following massive pulmonary embolism when anticipated benefits of conventional therapy are reduced Chronic, recurrent pulmonary embolism when anticoagulant therapy has failed or is contraindicated

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