Central Venous Catheter Kit - FDA Registration 4f3ce0f239f256603bc87ca2a62875be
Access comprehensive regulatory information for Central Venous Catheter Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4f3ce0f239f256603bc87ca2a62875be and manufactured by Guangdong Baihe Medical Technology Co.,Ltd.. The device was registered on March 10, 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
4f3ce0f239f256603bc87ca2a62875be
Central Venous Catheter Kit
FDA ID: 4f3ce0f239f256603bc87ca2a62875be
Device Classification
Brand Name
Vcath
Registration Information
Analysis ID
4f3ce0f239f256603bc87ca2a62875be
Registration Date
March 10, 2022
Manufacturer
Authorized Representative

