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Aspiration Needle - India CDSCO Medical Device Registration

Aspiration Needle is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000554_b498728e1605be3193d76fdb535fb874_88d35cf92fc4f329bd75bed987c080af. This device is marketed under the brand name ViziShot 2 Flex. The license holder is Olympus Medical Systems India Private Limited ,A-Block, 2nd Floor, Hafed Warehouse Complex, New Anaj Mandi, Khandsa Road ,Gurgaon Haryana ,122001 ,India, 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
Aspiration Needle
UID: IMP/MD/2020/000554_b498728e1605be3193d76fdb535fb874_88d35cf92fc4f329bd75bed987c080af

Brand Name

ViziShot 2 Flex

Device Class

Class B

Approving Authority

CDSCO

Product Information

This ViziShot 2 Flex has been designed to be used with an Olympus ultrasound endoscope for ultrasonic guide fine needle aspiration (ViziShot 2 Flex) and fine needle biopsy (ViziShot 2 Flex) of submucosal and extramural lesions of the tracheobronchial tree.

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