Myanmar FDA registration 4d009626ab47d49de6056537d03ebc7e

THE LATEX TEST KIT

Local name: LE LATEX TEST KIT

Myanmar·Lorne·Lorne Laboratories Limited·Registered August 27, 2022

Device classification

Brand Name: Lorne

Registration information

Analysis ID: 4d009626ab47d49de6056537d03ebc7e
Registration Date: August 27, 2022

Manufacturer

Name: Lorne Laboratories Limited

Authorized Representative

Name: DEW MEDICAL AND DIAGNOSTIC (DMD) COMPANY LIMITED

About this record

Access comprehensive regulatory information for THE LATEX TEST KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4d009626ab47d49de6056537d03ebc7e and manufactured by Lorne Laboratories Limited. The device was registered on August 27, 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.