Myanmar FDA registration 9fc580cf13f84ce2df5d58290472e9b8

Ureaplasma Urealyticum DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)

Myanmar·Sansure Biotech Inc.·Sansure Biotech Inc.·Registered September 21, 2022

Device classification

Brand Name: Sansure Biotech Inc.

Registration information

Analysis ID: 9fc580cf13f84ce2df5d58290472e9b8
Registration Date: September 21, 2022

Manufacturer

Name: Sansure Biotech Inc.

Authorized Representative

Name: BIOMED MYANMAR COMPANY LIMITED

About this record

Access comprehensive regulatory information for Ureaplasma Urealyticum DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9fc580cf13f84ce2df5d58290472e9b8 and manufactured by Sansure Biotech Inc.. The device was registered on September 21, 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.