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Hi-Torque Balance Middleweight Universal II Guide Wire - FDA Registration b7f82cc8a97baaf4a975cb45fbb5c127

Access comprehensive regulatory information for Hi-Torque Balance Middleweight Universal II Guide Wire in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b7f82cc8a97baaf4a975cb45fbb5c127 and manufactured by Abbott Vascular. The device was registered on August 18, 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
b7f82cc8a97baaf4a975cb45fbb5c127
Hi-Torque Balance Middleweight Universal II Guide Wire
FDA ID: b7f82cc8a97baaf4a975cb45fbb5c127
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Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
b7f82cc8a97baaf4a975cb45fbb5c127
Registration Date
August 18, 2022
Manufacturer
Authorized Representative