Pure Global

Biopsy Devices - India CDSCO Medical Device Registration

Biopsy Devices is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000059_5d9fa391085d43c59575ebb149cf26c9_735868f1adfaa60f5ef9fa232d09e558. This device is marketed under the brand name Interject Contrast Injection Therapy Needle Catheter. The license holder is Boston Scientific India Pvt. Ltd.,, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Biopsy Devices
UID: IMP/MD/2018/000059_5d9fa391085d43c59575ebb149cf26c9_735868f1adfaa60f5ef9fa232d09e558

Brand Name

Interject Contrast Injection Therapy Needle Catheter

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Multibite Multiple Sample Biopsy Forceps are designed specifically to collect tissue endoscopically for histologic examinations. These instruments are intended for endoscopic gastrointestinal biopsy and should not be used for any purpose other than their intended function

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing