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EMSCULPT NEO - FDA Registration 521f1a28448501e8568a70d20253f1ee

Access comprehensive regulatory information for EMSCULPT NEO in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 521f1a28448501e8568a70d20253f1ee and manufactured by BTL Industries. The device was registered on July 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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521f1a28448501e8568a70d20253f1ee
EMSCULPT NEO
FDA ID: 521f1a28448501e8568a70d20253f1ee
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Device Classification
Brand Name
BTL
Registration Information
Analysis ID
521f1a28448501e8568a70d20253f1ee
Registration Date
July 29, 2022
Manufacturer
Authorized Representative