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Procalcitonin Rapid Test - India CDSCO Medical Device Registration

Procalcitonin Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_73e123fa42dc7b845e6d14215ae2a9bf_a17a1d0a0e86c76fc5dec486910ec43c. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South 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
Procalcitonin Rapid Test
UID: MFG/IVD/2023/000113_73e123fa42dc7b845e6d14215ae2a9bf_a17a1d0a0e86c76fc5dec486910ec43c

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

This kit is used to detect the concentration of Procalcitonin (Chimera) in human serum for clinical diagnosis of bacterial infected diseases, via immunochromatographic technology

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