Myanmar FDA registration cd0c7ec3a091b4159ec266897113c845

Respiratory Humidifier

Name: Respiratory Humidifier — Myanmar FDA registration cd0c7ec3a091b4159ec266897113c845
Creator: VADI Medical Technology Co., Ltd. Yangmei
Keywords: Respiratory Humidifier, Respiratory Humidifier, VADI Brand, cd0c7ec3a091b4159ec266897113c845, Myanmar FDA registration

MyanmarVADI BrandVADI Medical Technology Co., Ltd. YangmeiRegistered September 21, 2022

VerifiedFDA Myanmar · official registry

Device classification

Brand Name: VADI Brand

Registration information

Analysis ID: cd0c7ec3a091b4159ec266897113c845
Registration Date: September 21, 2022

Manufacturer

Name: VADI Medical Technology Co., Ltd. Yangmei

Authorized Representative

Name: AMTT CO., LTD

About this record

Access comprehensive regulatory information for Respiratory Humidifier in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cd0c7ec3a091b4159ec266897113c845 and manufactured by VADI Medical Technology Co., Ltd. Yangmei. The device was registered on September 21, 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.