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Legionella - India CDSCO Medical Device Registration

Legionella is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000602_bdded704d3c4428571aaaa5f0211c515_4181c3542f6a77074ae58c9cbdc26694. This device is marketed under the brand name CERTEST STREP A. The license holder is KDH BIOMEDICALS PVT LTD, and it is classified as Device Class Class C. 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 C
Legionella
UID: IMP/IVD/2020/000602_bdded704d3c4428571aaaa5f0211c515_4181c3542f6a77074ae58c9cbdc26694

Brand Name

CERTEST STREP A

Device Class

Class C

Approving Authority

CDSCO

Product Information

For the qualitative detection of Legionella pneumophilla in human urine samples

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Products from the same license holder (10 products)

Adenovirus Resp

Brand: CERTEST STREP A

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Adenovirus

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FOB

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Calprotectin Turbilatex Sample Collection Vials

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Campylobacter

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H.Pylori

Brand: CERTEST STREP A

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