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Venous Implantable port - India CDSCO Medical Device Registration

Venous Implantable port is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000101_fb3e320f826279664f105b197f9afe07_f857ba0e3263dc0a43656f5a5df52c81. This device is marketed under the brand name Polythese POLYBRANCH. The license holder is VYGON INDIA PRIVATE LIMITED, 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
Venous Implantable port
UID: IMP/MD/2020/000101_fb3e320f826279664f105b197f9afe07_f857ba0e3263dc0a43656f5a5df52c81

Brand Name

Polythese POLYBRANCH

Device Class

Class D

Approving Authority

CDSCO

Product Information

A sterile implantable device intended to provide access to the peripheral arteries/veins for infusion (Polythese POLYBRANCH) and/or drainage (Polythese POLYBRANCH). It typically consists of a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle, attached to a distal catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Polythese POLYBRANCH)] and synthetic polymers (Polythese POLYBRANCH); disposable devices associated with implantation may be includedยป.)

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