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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_6933ec2d5d68601f35efad5b6d6be848. 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.

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CDSCO Registered
Class Class B
Biopsy Devices
UID: IMP/MD/2018/000059_5d9fa391085d43c59575ebb149cf26c9_6933ec2d5d68601f35efad5b6d6be848

Brand Name

Interject Contrast Injection Therapy Needle Catheter

Device Class

Class B

Approving Authority

CDSCO

Product Information

These single-use biopsy forceps are specifically designed to collect tissue endoscopically for histologic examination. These forceps should not be used for any purpose other than their intended function

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