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GLUCOSE PAP - India CDSCO Medical Device Registration

GLUCOSE PAP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000060_7aae1680a44a2e8dccda4f82b9b1fb34_09f7a58b7dc63c31e499d2c7f5b6459b. This device is marketed under the brand name a. The license holder is POCT Services Private Limited, and it is classified as Device Class Class B. The approving authority is North Delhi Division.

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
GLUCOSE PAP
UID: MFG/IVD/2021/000060_7aae1680a44a2e8dccda4f82b9b1fb34_09f7a58b7dc63c31e499d2c7f5b6459b

Brand Name

a

Device Class

Class B

Approving Authority

North Delhi Division

Product Information

Q-Lineโ„ข Glucose PAP is intended for the quantitative in vitro diagnostic etermination of Glucose in human samples of serum, plasma and urine

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