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Electric Craniotome (Electronic Power Drill),ELAN 4 ELECTRO BASIC SET CRANIO-SPINE - FDA Registration a5270c49afeb2afc743fdda096cf2ead

Access comprehensive regulatory information for Electric Craniotome (Electronic Power Drill),ELAN 4 ELECTRO BASIC SET CRANIO-SPINE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a5270c49afeb2afc743fdda096cf2ead and manufactured by Aesculap AG. The device was registered on December 02, 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
a5270c49afeb2afc743fdda096cf2ead
Electric Craniotome (Electronic Power Drill),ELAN 4 ELECTRO BASIC SET CRANIO-SPINE
FDA ID: a5270c49afeb2afc743fdda096cf2ead
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Device Classification
Brand Name
Aesculap
Registration Information
Analysis ID
a5270c49afeb2afc743fdda096cf2ead
Registration Date
December 02, 2022
Manufacturer
Authorized Representative