Myanmar FDA registration e5016080fd91861852cb81daaf32e339

Urea (UREA) Kit (Urease-GLDH Method)

Name: Urea (UREA) Kit (Urease-GLDH Method) — Myanmar FDA registration e5016080fd91861852cb81daaf32e339
Creator: Zybio Inc.
Keywords: Urea (UREA) Kit (Urease-GLDH Method), Urea (UREA) Kit (Urease-GLDH Method), Zybio Inc., e5016080fd91861852cb81daaf32e339, Myanmar FDA registration

MyanmarZybio Inc.Zybio Inc.Registered December 16, 2022

VerifiedFDA Myanmar · official registry

Device classification

Brand Name: Zybio Inc.

Registration information

Analysis ID: e5016080fd91861852cb81daaf32e339
Registration Date: December 16, 2022

Manufacturer

Name: Zybio Inc.

Authorized Representative

Name: BIOMED MYANMAR COMPANY LIMITED

About this record

Access comprehensive regulatory information for Urea (UREA) Kit (Urease-GLDH Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e5016080fd91861852cb81daaf32e339 and manufactured by Zybio Inc.. The device was registered on December 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.