Hollow Fiber Dialyzer - FDA Registration 43763f01fabbaf7e2b76736eb590fc18
Access comprehensive regulatory information for Hollow Fiber Dialyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 43763f01fabbaf7e2b76736eb590fc18 and manufactured by Shandong Weigao Blood Purification Products Co., Ltd.. The device was registered on April 28, 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
43763f01fabbaf7e2b76736eb590fc18
Hollow Fiber Dialyzer
FDA ID: 43763f01fabbaf7e2b76736eb590fc18
Device Classification
Brand Name
WEGO Brand
Registration Information
Analysis ID
43763f01fabbaf7e2b76736eb590fc18
Registration Date
April 28, 2022
Manufacturer
Authorized Representative

