Pure Global

AV Fistula Needle Set - India CDSCO Medical Device Registration

AV Fistula Needle Set is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000942_4ecc888adaebbc2cccca609e01796dce_d6e7a3306f9a1371cc00891bb59e3bfa. This device is marketed under the brand name Infusion Set Non-Vented Infuhope. The license holder is Arni Medica Private Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
AV Fistula Needle Set
UID: MFG/MD/2023/000942_4ecc888adaebbc2cccca609e01796dce_d6e7a3306f9a1371cc00891bb59e3bfa

Brand Name

Infusion Set Non-Vented Infuhope

Device Class

Class B

Approving Authority

Telangana

Product Information

AV Fistula needle set are indicated for use in conjunction with a connector of Haemodialysis blood tubing set. AV Fistula needle is a Connector to connect blood lines to the blood vessel through needle when dialysis is carried out via an internal fistula

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing