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RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE - FDA Registration IVDR-00532

Access comprehensive regulatory information for RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00532 and manufactured by Hangzhou AllTest Biotech Co., Ltd. - Hangzhou, People's Republic of China in China. The device was registered on November 06, 2020.

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-00532
RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE
Registered medical device in Philippines
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Device Information
Product Name
RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE
Registration Number
IVDR-00532
Manufacturer Details
Country of Origin
China
Importer & Distribution
Importer/Distributor
Iraseth Pharma Inc.
Registration Dates
Issuance Date
November 06, 2020
Expiry Date
November 06, 2021