Myanmar FDA registration 2025c02bb5b880e3e4ac44cba6611584

LIQUID ASSAYED SPECIFIC PROTEIN - CONTROL LEVEL 3 (SP CONTROL 3)

Myanmar·Randox·Randox Laboratories Ltd.·Registered April 28, 2022

Device classification

Brand Name: Randox

Registration information

Analysis ID: 2025c02bb5b880e3e4ac44cba6611584
Registration Date: April 28, 2022

Manufacturer

Name: Randox Laboratories Ltd.

Authorized Representative

Name: BIOMED MYANMAR COMPANY LIMITED

About this record

Access comprehensive regulatory information for LIQUID ASSAYED SPECIFIC PROTEIN - CONTROL LEVEL 3 (SP CONTROL 3) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2025c02bb5b880e3e4ac44cba6611584 and manufactured by Randox Laboratories Ltd.. The device was registered on April 28, 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.