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Ultimaster Sirolimus Eluting Coronary Stent System (TERUMO Brand) - FDA Registration 10c1e55313c84539fd9b8a6895e97139

Access comprehensive regulatory information for Ultimaster Sirolimus Eluting Coronary Stent System (TERUMO Brand) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 10c1e55313c84539fd9b8a6895e97139 and manufactured by Ashitaka Factory of Terumo Corporation. 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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10c1e55313c84539fd9b8a6895e97139
Ultimaster Sirolimus Eluting Coronary Stent System (TERUMO Brand)
FDA ID: 10c1e55313c84539fd9b8a6895e97139
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Device Classification
Brand Name
TERUMO
Registration Information
Analysis ID
10c1e55313c84539fd9b8a6895e97139
Registration Date
November 10, 2022
Authorized Representative