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Lifecheck One Step HCG Urine/Serum Test - FDA Registration IVDR-00742

Access comprehensive regulatory information for Lifecheck One Step HCG Urine/Serum Test in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00742 and manufactured by Guangzhou Wondfo Biotech Co., Ltd. No. 8 Lizhishan Road, Science City, Luogang District, 510663, Guangzhou, P.R. China in China. The device was registered on March 17, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Allied Hospital Supply International Corporation), 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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IVDR-00742
Lifecheck One Step HCG Urine/Serum Test
Registered medical device in Philippines
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Device Information
Product Name
Lifecheck One Step HCG Urine/Serum Test
Registration Number
IVDR-00742
Importer & Distribution
Registration Dates
Issuance Date
March 17, 2023
Expiry Date
March 17, 2024