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Dual Top Anchor System ( Bone Plate ) - FDA Registration 4097fdacbfc33eaeec4f9a2b9e64cf1b

Access comprehensive regulatory information for Dual Top Anchor System ( Bone Plate ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4097fdacbfc33eaeec4f9a2b9e64cf1b and manufactured by Jeil Medical Corporation. The device was registered on July 11, 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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4097fdacbfc33eaeec4f9a2b9e64cf1b
Dual Top Anchor System ( Bone Plate )
FDA ID: 4097fdacbfc33eaeec4f9a2b9e64cf1b
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Device Classification
Brand Name
JEIL MEDICAL
Registration Information
Analysis ID
4097fdacbfc33eaeec4f9a2b9e64cf1b
Registration Date
July 11, 2022
Manufacturer
Authorized Representative