Transcutaneous Jaundice Detector - FDA Registration 187d901d42f992b1e38d72196604f071
Access comprehensive regulatory information for Transcutaneous Jaundice Detector in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 187d901d42f992b1e38d72196604f071 and manufactured by Ningbo David Medical Device Co.,Ltd.. The device was registered on September 16, 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
187d901d42f992b1e38d72196604f071
Transcutaneous Jaundice Detector
FDA ID: 187d901d42f992b1e38d72196604f071
Device Classification
Brand Name
DAVID
Registration Information
Analysis ID
187d901d42f992b1e38d72196604f071
Registration Date
September 16, 2022
Manufacturer
Authorized Representative

