Myanmar FDA registration defd40bf0423ab67b437f67cae531499
CRP Direct Latex
Device classification
- Brand Name
- CRP DIRECT LATEX
Registration information
- Analysis ID
- defd40bf0423ab67b437f67cae531499
- Registration Date
- November 02, 2022
Manufacturer
- Name
- VEDA . LAB
Authorized Representative
About this record
Access comprehensive regulatory information for CRP Direct Latex in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID defd40bf0423ab67b437f67cae531499 and manufactured by VEDA . LAB. The device was registered on November 02, 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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