A.V.FISTULA NEEDLE SET FOR SINGLE USE - FDA Registration 6f726aa60746f9549e45b4a3c52f4e9a
Access comprehensive regulatory information for A.V.FISTULA NEEDLE SET FOR SINGLE USE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6f726aa60746f9549e45b4a3c52f4e9a and manufactured by Jiangxi Sanxin Medtec Co.,Ltd.PR.China.. The device was registered on August 15, 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
6f726aa60746f9549e45b4a3c52f4e9a
A.V.FISTULA NEEDLE SET FOR SINGLE USE
FDA ID: 6f726aa60746f9549e45b4a3c52f4e9a
Device Classification
Brand Name
Hanma
Registration Information
Analysis ID
6f726aa60746f9549e45b4a3c52f4e9a
Registration Date
August 15, 2022
Manufacturer
Authorized Representative

