PEPA Dialyzer FDX - FDA Registration e3377bcfd734948a0e36f99ad64ec0ce
Access comprehensive regulatory information for PEPA Dialyzer FDX in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e3377bcfd734948a0e36f99ad64ec0ce and manufactured by Nikkiso Co.,ltd.. The device was registered on March 01, 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
e3377bcfd734948a0e36f99ad64ec0ce
PEPA Dialyzer FDX
FDA ID: e3377bcfd734948a0e36f99ad64ec0ce
Device Classification
Brand Name
Nikkiso Brand
Registration Information
Analysis ID
e3377bcfd734948a0e36f99ad64ec0ce
Registration Date
March 01, 2022
Manufacturer
Name
Nikkiso Co.,ltd.Authorized Representative

