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Dual Curing Resin Based Luting Cement - FDA Registration 6ab3bc3af82fe1646bb0b959122129ed

Access comprehensive regulatory information for Dual Curing Resin Based Luting Cement in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6ab3bc3af82fe1646bb0b959122129ed and manufactured by Prevest DenPro Limited. The device was registered on May 14, 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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6ab3bc3af82fe1646bb0b959122129ed
Dual Curing Resin Based Luting Cement
FDA ID: 6ab3bc3af82fe1646bb0b959122129ed
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Device Classification
Brand Name
FUSION ULTRA D/C
Registration Information
Analysis ID
6ab3bc3af82fe1646bb0b959122129ed
Registration Date
May 14, 2022
Manufacturer
Authorized Representative