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AV Fistula Needle - FDA Registration 64dd94c61112ccbba19ec8826ae4cbbc

Access comprehensive regulatory information for AV Fistula Needle in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 64dd94c61112ccbba19ec8826ae4cbbc and manufactured by PT. Nipro Indonesia Jaya,. The device was registered on August 29, 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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64dd94c61112ccbba19ec8826ae4cbbc
AV Fistula Needle
FDA ID: 64dd94c61112ccbba19ec8826ae4cbbc
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Device Classification
Brand Name
Nipro
Registration Information
Analysis ID
64dd94c61112ccbba19ec8826ae4cbbc
Registration Date
August 29, 2022
Authorized Representative