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Antisera - FDA Registration db575cfc568962a680970bc15877f147

Access comprehensive regulatory information for Antisera in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID db575cfc568962a680970bc15877f147 and manufactured by Lab-Care Diagnostics (India) Pvt. Ltd.. The device was registered on November 09, 2022.

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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db575cfc568962a680970bc15877f147
Antisera
FDA ID: db575cfc568962a680970bc15877f147
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Device Classification
Brand Name
SHUBHAM
Registration Information
Analysis ID
db575cfc568962a680970bc15877f147
Registration Date
November 09, 2022