SHEATH - FDA Registration b90678761fa7de13f5b436626248a0c6
Access comprehensive regulatory information for SHEATH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b90678761fa7de13f5b436626248a0c6 and manufactured by URIT Medical Electronic Co., Ltd.,. The device was registered on December 21, 2021.
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 Database
Powered by Pure Global AI
FDA Official Data
b90678761fa7de13f5b436626248a0c6
SHEATH
FDA ID: b90678761fa7de13f5b436626248a0c6
Device Classification
Brand Name
URIT Brand
Registration Information
Analysis ID
b90678761fa7de13f5b436626248a0c6
Registration Date
December 21, 2021
Manufacturer
Authorized Representative
Name
AMTT CO., LTD
