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Cobas 8000 Additional ISE Kit - India CDSCO Medical Device Registration

Cobas 8000 Additional ISE Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000406_cac21074b30b19934006b67ea81f129e_d99b81173677be07398eae366e152537. This device is marketed under the brand name Cobas pro SB. The license holder is Roche Diagnostics India Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Cobas 8000 Additional ISE Kit
UID: IMP/IVD/2022/000406_cac21074b30b19934006b67ea81f129e_d99b81173677be07398eae366e152537

Brand Name

Cobas pro SB

Device Class

Class A

Approving Authority

CDSCO

Product Information

The cobas 8000 Additional ISE KIT is an IVD accessory used for the modification from ISE 900 module to ISE 1800 module at cobas 8000 modular analyzer series

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