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KINEVO 900 - India CDSCO Medical Device Registration

KINEVO 900 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000320_be855f13b69a6a73e08168df3ef4f6cb_3d0aef341632df25d34e9e6c85e7b950. This device is marketed under the brand name ZEISS. The license holder is Carl Zeiss India (Bangalore) 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
KINEVO 900
UID: IMP/MD/2023/000320_be855f13b69a6a73e08168df3ef4f6cb_3d0aef341632df25d34e9e6c85e7b950

Brand Name

ZEISS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The KINEVO 900 is a surgical microscope intended for the illumination and magnification of the surgical area and for the support of visualization in surgical procedures.

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