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RETIC TUBE - India CDSCO Medical Device Registration

RETIC TUBE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000124_f58ea0d01a9d72fc55c243c44ccab355_d7dc7546a05501270071cb1ee6378ef4. This device is marketed under the brand name BONAVERA ESR TUBE. The license holder is Biogeny Diagnostics Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is Gujarat.

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 A
RETIC TUBE
UID: MFG/IVD/2020/000124_f58ea0d01a9d72fc55c243c44ccab355_d7dc7546a05501270071cb1ee6378ef4

Brand Name

BONAVERA ESR TUBE

Device Class

Class A

Approving Authority

Gujarat

Product Information

for reticulocyte cell count determination of blood sample in haematology

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