Myanmar FDA registration 2f1c37167f5d0308dcc433dcc9072809
Hemoglobin Analyzer (HPLC)
Device classification
- Brand Name
- Lifotronic
Registration information
- Analysis ID
- 2f1c37167f5d0308dcc433dcc9072809
- Registration Date
- December 09, 2021
Manufacturer
Authorized Representative
- Name
- GAMBIRO CO., LTD
About this record
Access comprehensive regulatory information for Hemoglobin Analyzer (HPLC) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2f1c37167f5d0308dcc433dcc9072809 and manufactured by Shenzhen Lifotronic Technology Co.,Ltd. The device was registered on December 09, 2021.
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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