Manifold - FDA Registration fbffb6ed418c4eeacaf659e869f3343c
Access comprehensive regulatory information for Manifold in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fbffb6ed418c4eeacaf659e869f3343c and manufactured by Merit Medical Systems,Inc.. 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.
Free Database
Powered by Pure Global AI
FDA Official Data
fbffb6ed418c4eeacaf659e869f3343c
Manifold
FDA ID: fbffb6ed418c4eeacaf659e869f3343c
Device Classification
Brand Name
Merit Medical
Registration Information
Analysis ID
fbffb6ed418c4eeacaf659e869f3343c
Registration Date
March 14, 2022
Manufacturer
Authorized Representative

