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Terufusion Syringe Pump SS3 - FDA Registration 5330aec23a15e70738a061841ceccd9d

Access comprehensive regulatory information for Terufusion Syringe Pump SS3 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5330aec23a15e70738a061841ceccd9d and manufactured by Ashitaka Factory of Terumo Corporation. The device was registered on July 26, 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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5330aec23a15e70738a061841ceccd9d
Terufusion Syringe Pump SS3
FDA ID: 5330aec23a15e70738a061841ceccd9d
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Device Classification
Brand Name
Terumo
Registration Information
Analysis ID
5330aec23a15e70738a061841ceccd9d
Registration Date
July 26, 2022