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MNCHIP reagents - FDA Registration 05483cc144f37cf98530eb52386a24e5

Access comprehensive regulatory information for MNCHIP reagents in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 05483cc144f37cf98530eb52386a24e5 and manufactured by Tianjin MNCHIP Technologies Co., Ltd. The device was registered on December 21, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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05483cc144f37cf98530eb52386a24e5
MNCHIP reagents
FDA ID: 05483cc144f37cf98530eb52386a24e5
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Device Classification
Brand Name
MNCHIP
Registration Information
Analysis ID
05483cc144f37cf98530eb52386a24e5
Registration Date
December 21, 2021
Authorized Representative