Philippines FDA registration IVDR-00532

RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE

Philippines·Hangzhou AllTest Biotech Co., Ltd. - Hangzhou, People's Republic of China·China·Issued November 06, 2020 – November 06, 2021

Device information

Product Name: RAPIQUICK LEPTOSPIRA RAPID TEST DEVICE
Registration Number: IVDR-00532

Manufacturer details

Manufacturer: Hangzhou AllTest Biotech Co., Ltd. - Hangzhou, People's Republic of China
Country of Origin: China

Importer & distribution

Importer/Distributor: Iraseth Pharma Inc.

Registration dates

Issuance Date: November 06, 2020
Expiry Date: November 06, 2021

About this record

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.