Viatrac 14 Plus Peripheral Dilatation Catheter - FDA Registration b46a307535cf4ccca437e4379cbf651c
Access comprehensive regulatory information for Viatrac 14 Plus Peripheral Dilatation Catheter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b46a307535cf4ccca437e4379cbf651c and manufactured by Abbott Vascular. The device was registered on May 13, 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
b46a307535cf4ccca437e4379cbf651c
Viatrac 14 Plus Peripheral Dilatation Catheter
FDA ID: b46a307535cf4ccca437e4379cbf651c
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
b46a307535cf4ccca437e4379cbf651c
Registration Date
May 13, 2022
Manufacturer
Name
Abbott VascularAuthorized Representative

