Pure Global
Myanmar FDA registration 0c6f3101fbb418b424582e5e1b9326c6

Visalis 500 and accessories

Myanmar flagMyanmar·Carl Zeiss·Carl Zeiss Meditec AG·Registered March 31, 2022
Device classification
Brand Name
Carl Zeiss
Registration information
Analysis ID
0c6f3101fbb418b424582e5e1b9326c6
Registration Date
March 31, 2022
Manufacturer
Name
Carl Zeiss Meditec AG
Authorized Representative
Name
MYANMAR AMERICAN VISION COMPANY LIMITED
About this record

Access comprehensive regulatory information for Visalis 500 and accessories in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0c6f3101fbb418b424582e5e1b9326c6 and manufactured by Carl Zeiss Meditec AG. The device was registered on March 31, 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.

Free DatabasePowered by Pure Global AIFDA Official Data