HOSPI PLUS aspirator - FDA Registration 52602f5e4690988807a99dd306cf1264
Access comprehensive regulatory information for HOSPI PLUS aspirator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 52602f5e4690988807a99dd306cf1264 and manufactured by Gima S.p.A.. The device was registered on December 09, 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
52602f5e4690988807a99dd306cf1264
HOSPI PLUS aspirator
FDA ID: 52602f5e4690988807a99dd306cf1264
Device Classification
Brand Name
GIMA
Registration Information
Analysis ID
52602f5e4690988807a99dd306cf1264
Registration Date
December 09, 2022
Manufacturer
Name
Gima S.p.A.Authorized Representative

