SCALP VEIN SET - FDA Registration 4182f5cfc1e8388e39c5adfb1086f84d
Access comprehensive regulatory information for SCALP VEIN SET in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4182f5cfc1e8388e39c5adfb1086f84d and manufactured by Yangzhou Medline Industry Co.,Ltd.. The device was registered on October 06, 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
4182f5cfc1e8388e39c5adfb1086f84d
SCALP VEIN SET
FDA ID: 4182f5cfc1e8388e39c5adfb1086f84d
Device Classification
Brand Name
AM Care
Registration Information
Analysis ID
4182f5cfc1e8388e39c5adfb1086f84d
Registration Date
October 06, 2022
Manufacturer
Authorized Representative

