WIDAL SLIDE TEST - FDA Registration ba635a0bc81a95db7b422a5a5545e233
Access comprehensive regulatory information for WIDAL SLIDE TEST in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ba635a0bc81a95db7b422a5a5545e233 and manufactured by Lab-Care Diagnostics (I) Pvt. Ltd.. The device was registered on December 01, 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
ba635a0bc81a95db7b422a5a5545e233
WIDAL SLIDE TEST
FDA ID: ba635a0bc81a95db7b422a5a5545e233
Device Classification
Brand Name
SHUBHAM
Registration Information
Analysis ID
ba635a0bc81a95db7b422a5a5545e233
Registration Date
December 01, 2022
Manufacturer
Authorized Representative

