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C-Peptide Testing Kit - India CDSCO Medical Device Registration

C-Peptide Testing Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000001_c31874a9a8343edfeff6ffb02d15edc6_bf137bbfbcbe1a1887f02db6c9c640aa. This device is marketed under the brand name Lumella. The license holder is Diabetomics Medical (P) Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
C-Peptide Testing Kit
UID: MFG/IVD/2019/000001_c31874a9a8343edfeff6ffb02d15edc6_bf137bbfbcbe1a1887f02db6c9c640aa

Brand Name

Lumella

Device Class

Class B

Approving Authority

Telangana

Product Information

The Insudexยฎ C-Peptide test kit is intended to be an aid in the diagnosis of patients with abnormal insulin secretion by quantitative determination of C-peptide in human serum

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