Myanmar FDA registration a0c4d90adfdcb27b1595870f5fe63c34

Rapid Latex Kit

Myanmar·Lorne·Lorne Laboratories Ltd·Registered September 01, 2022

Device classification

Brand Name: Lorne

Registration information

Analysis ID: a0c4d90adfdcb27b1595870f5fe63c34
Registration Date: September 01, 2022

Manufacturer

Name: Lorne Laboratories Ltd

Authorized Representative

Name: DEW MEDICAL AND DIAGNOSTIC (DMD) COMPANY LIMITED

About this record

Access comprehensive regulatory information for Rapid Latex Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a0c4d90adfdcb27b1595870f5fe63c34 and manufactured by Lorne Laboratories Ltd. The device was registered on September 01, 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.