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Hi-Torque Whisper Guide Wire - FDA Registration 3ed8b2e7d14eef66cf8b9302c21d794b

Access comprehensive regulatory information for Hi-Torque Whisper Guide Wire in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3ed8b2e7d14eef66cf8b9302c21d794b 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
3ed8b2e7d14eef66cf8b9302c21d794b
Hi-Torque Whisper Guide Wire
FDA ID: 3ed8b2e7d14eef66cf8b9302c21d794b
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Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
3ed8b2e7d14eef66cf8b9302c21d794b
Registration Date
August 18, 2022
Manufacturer
Authorized Representative