Electrocardiovit (ECG) - FDA Registration 34f6b58cd59cf5310ae2c8346c4046b3
Access comprehensive regulatory information for Electrocardiovit (ECG) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 34f6b58cd59cf5310ae2c8346c4046b3 and manufactured by Schiller AG. The device was registered on February 01, 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
34f6b58cd59cf5310ae2c8346c4046b3
Electrocardiovit (ECG)
FDA ID: 34f6b58cd59cf5310ae2c8346c4046b3
Device Classification
Brand Name
Schiller
Registration Information
Analysis ID
34f6b58cd59cf5310ae2c8346c4046b3
Registration Date
February 01, 2022
Manufacturer
Name
Schiller AGAuthorized Representative

