Pure Global

Polyethersulphone Hallow Fiber Hemodialyzer - India CDSCO Medical Device Registration

Polyethersulphone Hallow Fiber Hemodialyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000577_4fbaee91e911b6e0df58117c2dc5e6bc_debabe1033d89e9111b649aebaf12537. This device is marketed under the brand name Purifier. The license holder is M/s LepuCare (India) Vascular Solutions Pvt. Ltd.,, and it is classified as Device Class Class C. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Polyethersulphone Hallow Fiber Hemodialyzer
UID: IMP/MD/2021/000577_4fbaee91e911b6e0df58117c2dc5e6bc_debabe1033d89e9111b649aebaf12537

Brand Name

Purifier

Device Class

Class C

Approving Authority

CDSCO

Product Information

OCI Polyethersulfone Hallow Fiber Hemodialyzer are designed for single use in acute and chronic renal failure hemodialysis.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing