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RAPIQUICK DRUG OF ABUSE 5 IN 1 TEST KIT DEVICE ONE STEP RAPID TEST DEVICE FOR THC50/MET1000/MDMA500/COC300/MOP2000 - FDA Registration IVDR-00638

Access comprehensive regulatory information for RAPIQUICK DRUG OF ABUSE 5 IN 1 TEST KIT DEVICE ONE STEP RAPID TEST DEVICE FOR THC50/MET1000/MDMA500/COC300/MOP2000 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00638 and manufactured by Hangzhou AllTest Biotech Co., Ltd. - Hangzhou, People's Republic of China in China. The device was registered on October 11, 2021.

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-00638
RAPIQUICK DRUG OF ABUSE 5 IN 1 TEST KIT DEVICE ONE STEP RAPID TEST DEVICE FOR THC50/MET1000/MDMA500/COC300/MOP2000
Registered medical device in Philippines
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Device Information
Product Name
RAPIQUICK DRUG OF ABUSE 5 IN 1 TEST KIT DEVICE ONE STEP RAPID TEST DEVICE FOR THC50/MET1000/MDMA500/COC300/MOP2000
Registration Number
IVDR-00638
Manufacturer Details
Importer & Distribution
Importer/Distributor
Iraseth Pharma Inc.
Registration Dates
Issuance Date
October 11, 2021
Expiry Date
October 11, 2022