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LH Ovulation Rapid Test Cassette (Urine) - FDA Registration a62d924b3f8b169597742a7d1e68fc3f

Access comprehensive regulatory information for LH Ovulation Rapid Test Cassette (Urine) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a62d924b3f8b169597742a7d1e68fc3f and manufactured by Hangzhou AllTest Biotech Co., Ltd. The device was registered on October 17, 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
a62d924b3f8b169597742a7d1e68fc3f
LH Ovulation Rapid Test Cassette (Urine)
FDA ID: a62d924b3f8b169597742a7d1e68fc3f
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DJ Fang

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Device Classification
Brand Name
EMC Brand
Registration Information
Analysis ID
a62d924b3f8b169597742a7d1e68fc3f
Registration Date
October 17, 2022
Authorized Representative