Philippines FDA registration IVDR-00733

Trimera™ Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma)

Philippines flagPhilippines·Hangzhou AllTest Biotech Co., Ltd.- 550#, Yinhai Street Hangzhou Economic and Technological Development Area 310018 Hangzhou People's Republic of China·China·Issued October 18, 2024 – February 02, 2029
Device information
Product Name
Trimera™ Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma)
Registration Number
IVDR-00733
Manufacturer details
Country of Origin
China
Importer & distribution
Importer/Distributor
Chemtech Medical Supply
Registration dates
Issuance Date
October 18, 2024
Expiry Date
February 02, 2029
About this record

Access comprehensive regulatory information for Trimera™ Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00733 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 October 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Chemtech Medical Supply), 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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