Myanmar FDA registration 088cfcf32783b6ee9d874ad515340614
eCL8000 System
Myanmar·Lifotronic·Shenzhen Lifotronic Technology Co., Ltd·Registered March 27, 2022Device classification
- Brand Name
- Lifotronic
Registration information
- Analysis ID
- 088cfcf32783b6ee9d874ad515340614
- Registration Date
- March 27, 2022
Manufacturer
Authorized Representative
- Name
- GAMBIRO CO., LTD
About this record
Access comprehensive regulatory information for eCL8000 System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 088cfcf32783b6ee9d874ad515340614 and manufactured by Shenzhen Lifotronic Technology Co., Ltd. The device was registered on March 27, 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.
Free DatabasePowered by Pure Global AIFDA Official Data