Myanmar FDA registration bad1abde79f59ec4ddea06c372701386

LH Rapid Quantitative Test

Myanmar·Finecare·Guangzhou Wondfo Biotech Co., Ltd.·Registered September 09, 2022

Device classification

Brand Name: Finecare

Registration information

Analysis ID: bad1abde79f59ec4ddea06c372701386
Registration Date: September 09, 2022

Manufacturer

Name: Guangzhou Wondfo Biotech Co., Ltd.

Authorized Representative

Name: EVER GLORY COMPANY LIMITED

About this record

Access comprehensive regulatory information for LH Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bad1abde79f59ec4ddea06c372701386 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on September 09, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.