Myanmar FDA registration 08d9c2e1483c4bbc1a88e297bef6587e

CEA Rapid Quantitative Test

Myanmar·Finecare·Guangzhou Wondfo Biotech Co., Ltd.·Registered August 16, 2022

Device classification

Brand Name: Finecare

Registration information

Analysis ID: 08d9c2e1483c4bbc1a88e297bef6587e
Registration Date: August 16, 2022

Manufacturer

Name: Guangzhou Wondfo Biotech Co., Ltd.

Authorized Representative

Name: EVER GLORY COMPANY LIMITED

About this record

Access comprehensive regulatory information for CEA Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 08d9c2e1483c4bbc1a88e297bef6587e and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on August 16, 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.