ASAHI Peripheral Guide Wire - FDA Registration 62218f97d2d80dcc010291195dd8124a
Access comprehensive regulatory information for ASAHI Peripheral Guide Wire in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 62218f97d2d80dcc010291195dd8124a and manufactured by ASAHI INTECC (THAILAND) CO.,LTD. The device was registered on December 29, 2021.
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
62218f97d2d80dcc010291195dd8124a
ASAHI Peripheral Guide Wire
FDA ID: 62218f97d2d80dcc010291195dd8124a
Device Classification
Brand Name
ASAHI INTECC
Registration Information
Analysis ID
62218f97d2d80dcc010291195dd8124a
Registration Date
December 29, 2021
Manufacturer
Authorized Representative

