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Synicem Cranioplastie - FDA Registration 4f89ea9bd4b37f8e17d153197e7cc392

Access comprehensive regulatory information for Synicem Cranioplastie in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4f89ea9bd4b37f8e17d153197e7cc392 and manufactured by SYNIMED (Synergie Ingenierie Medicale) S.A.R.L. The device was registered on November 16, 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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4f89ea9bd4b37f8e17d153197e7cc392
Synicem Cranioplastie
FDA ID: 4f89ea9bd4b37f8e17d153197e7cc392
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Device Classification
Brand Name
Synimed
Registration Information
Analysis ID
4f89ea9bd4b37f8e17d153197e7cc392
Registration Date
November 16, 2022