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ELAN 4 TURNABLE DURAGUARD STANDARD - FDA Registration e5f4f53b4ea97f8395bd4ed32c897fe0

Access comprehensive regulatory information for ELAN 4 TURNABLE DURAGUARD STANDARD in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e5f4f53b4ea97f8395bd4ed32c897fe0 and manufactured by Aesculap AG. The device was registered on November 10, 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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FDA Official Data
e5f4f53b4ea97f8395bd4ed32c897fe0
ELAN 4 TURNABLE DURAGUARD STANDARD
FDA ID: e5f4f53b4ea97f8395bd4ed32c897fe0
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Device Classification
Brand Name
Aesculap
Registration Information
Analysis ID
e5f4f53b4ea97f8395bd4ed32c897fe0
Registration Date
November 10, 2022
Manufacturer
Authorized Representative