Philippines FDA registration IVDR-00787

iFlash HCG

Philippines·Shenzhen Yhlo Biotech Co., Ltd. Building 1, YHLO Biopark, Baolong 2nd Road, Baolong Subdistrict, Longgang District, 518116 Shenzhen, People's Republic of China·China·Issued January 03, 2024 – January 03, 2025

Device information

Product Name: iFlash HCG
Registration Number: IVDR-00787

Manufacturer details

Manufacturer: Shenzhen Yhlo Biotech Co., Ltd. Building 1, YHLO Biopark, Baolong 2nd Road, Baolong Subdistrict, Longgang District, 518116 Shenzhen, People's Republic of China
Country of Origin: China

Importer & distribution

Importer/Distributor: Lifeline Diagnostics Supplies, Inc.

Registration dates

Issuance Date: January 03, 2024
Expiry Date: January 03, 2025

About this record

Access comprehensive regulatory information for iFlash HCG in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00787 and manufactured by Shenzhen Yhlo Biotech Co., Ltd. Building 1, YHLO Biopark, Baolong 2nd Road, Baolong Subdistrict, Longgang District, 518116 Shenzhen, People's Republic of China in China. The device was registered on January 03, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifeline Diagnostics Supplies, 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.