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Myanmar FDA registration b1fffbcfc5e0a069ad7b3d7e24cea9b0

ARCHITECT Rubella IgM Reagent Kit

Myanmar flagMyanmar·Abbott·Abbott Ireland Diagnostics Division·Registered February 05, 2022
Device classification
Brand Name
Abbott
Registration information
Analysis ID
b1fffbcfc5e0a069ad7b3d7e24cea9b0
Registration Date
February 05, 2022
Manufacturer
Name
Abbott Ireland Diagnostics Division
Authorized Representative
Name
SEA LION COMPANY LIMITED
About this record

Access comprehensive regulatory information for ARCHITECT Rubella IgM Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b1fffbcfc5e0a069ad7b3d7e24cea9b0 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on February 05, 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.

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