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Rapiquick hCG (Human Chorionic Gonadotropin) Pregnancy Rapid Test - FDA Registration IVDR-00569

Access comprehensive regulatory information for Rapiquick hCG (Human Chorionic Gonadotropin) Pregnancy Rapid Test in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00569 and manufactured by Hangzhou AllTest Biotech Co., Ltd. 550#, Yinhai Street Hangzhou Economic and Technological Development Area 310018 Hangzhou People's Republic of China in China. The device was registered on April 27, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Iraseth Pharma Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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China
IVDR-00569
Rapiquick hCG (Human Chorionic Gonadotropin) Pregnancy Rapid Test
Registered medical device in Philippines
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Device Information
Product Name
Rapiquick hCG (Human Chorionic Gonadotropin) Pregnancy Rapid Test
Registration Number
IVDR-00569
Importer & Distribution
Importer/Distributor
Iraseth Pharma Inc.
Registration Dates
Issuance Date
April 27, 2023
Expiry Date
April 19, 2027