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Philippines FDA registration IVDR-00923

iCheck Tetrahydrocannabinol (THC) Rapid Test Cassette (Urine)

PhilippinesHangzhou AllTest Biotech Co., Ltd.ChinaIssued February 13, 2025 – February 13, 2026
VerifiedFDA Philippines · official registry
Device information
Product Name
iCheck Tetrahydrocannabinol (THC) Rapid Test Cassette (Urine)
Registration Number
IVDR-00923
Manufacturer details
Country of Origin
China
Importer & distribution
Registration dates
Issuance Date
February 13, 2025
Expiry Date
February 13, 2026
About this record

Access comprehensive regulatory information for iCheck Tetrahydrocannabinol (THC) Rapid Test Cassette (Urine) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00923 and manufactured by Hangzhou AllTest Biotech Co., Ltd. in China. The device was registered on February 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Philippine Blue Cross Biotech 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.