Vein-O-Line - FDA Registration d7bdbff183557dad3bc655dbf2dc4d32
Access comprehensive regulatory information for Vein-O-Line in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d7bdbff183557dad3bc655dbf2dc4d32 and manufactured by Romsons International (Unit-II). The device was registered on March 14, 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
d7bdbff183557dad3bc655dbf2dc4d32
Vein-O-Line
FDA ID: d7bdbff183557dad3bc655dbf2dc4d32
Device Classification
Brand Name
Romsons
Registration Information
Analysis ID
d7bdbff183557dad3bc655dbf2dc4d32
Registration Date
March 14, 2022
Manufacturer
Authorized Representative

