Myanmar FDA registration c229470f61a7114603c6171a0fc60023

Ultra HDL (ARCHITECT)

Myanmar·Abbott·Sekisui Diagnostics P.E.I. Inc.·Registered October 06, 2022

Device classification

Brand Name: Abbott

Registration information

Analysis ID: c229470f61a7114603c6171a0fc60023
Registration Date: October 06, 2022

Manufacturer

Name: Sekisui Diagnostics P.E.I. Inc.

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for Ultra HDL (ARCHITECT) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c229470f61a7114603c6171a0fc60023 and manufactured by Sekisui Diagnostics P.E.I. Inc.. The device was registered on October 06, 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.