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Transvaginal Access Platform - India CDSCO Medical Device Registration

Transvaginal Access Platform is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000936_652e0746c69cb5ea50f4bfdd87d6a242_369a659e7fb4331db5c967a8c2c078b1. This device is marketed under the brand name Kii Access Systems. The license holder is Digimed, 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
Transvaginal Access Platform
UID: IMP/MD/2023/000936_652e0746c69cb5ea50f4bfdd87d6a242_369a659e7fb4331db5c967a8c2c078b1

Brand Name

Kii Access Systems

License Holder

Digimed

Device Class

Class B

Approving Authority

CDSCO

Product Information

The GelPOINT V-Path Transvaginal Access Platform is intended to be inserted transvaginally to establish a path of entry for minimally invasive instruments while maintaining insufflation during laparoscopic assisted and vaginal gynecological procedures. The device is also a conduit for the extraction of specimens.

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