A.V FISTULA NEEDLE SET - FDA Registration 3ac65594563c9c7bf59dba18740936b8
Access comprehensive regulatory information for A.V FISTULA NEEDLE SET in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3ac65594563c9c7bf59dba18740936b8 and manufactured by SUNDER BIOMEDICAL TECH Co.,ltd. The device was registered on December 09, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
3ac65594563c9c7bf59dba18740936b8
A.V FISTULA NEEDLE SET
FDA ID: 3ac65594563c9c7bf59dba18740936b8
Device Classification
Brand Name
SUNDER BRAND
Registration Information
Analysis ID
3ac65594563c9c7bf59dba18740936b8
Registration Date
December 09, 2021
Manufacturer
Authorized Representative

