Myanmar FDA registration 5f17aee5b0b777d9764ce84a94082ec1
Video Duodenoscope
Myanmar·Pentax Medical·Hoya Corporation PENTAX Miyagi Factory·Registered July 20, 2022Device classification
- Brand Name
- Pentax Medical
Registration information
- Analysis ID
- 5f17aee5b0b777d9764ce84a94082ec1
- Registration Date
- July 20, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Video Duodenoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5f17aee5b0b777d9764ce84a94082ec1 and manufactured by Hoya Corporation PENTAX Miyagi Factory. The device was registered on July 20, 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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