Myanmar FDA registration c312bcfb0dc01eef67aea0db19e97ee9

Humidifier Chamber

Name: Humidifier Chamber — Myanmar FDA registration c312bcfb0dc01eef67aea0db19e97ee9
Creator: VADI Medical Technology Co., Ltd. Yangmei
Keywords: Humidifier Chamber, Humidifier Chamber, VADI Brand, c312bcfb0dc01eef67aea0db19e97ee9, Myanmar FDA registration

MyanmarVADI BrandVADI Medical Technology Co., Ltd. YangmeiRegistered August 22, 2022

VerifiedFDA Myanmar · official registry

Device classification

Brand Name: VADI Brand

Registration information

Analysis ID: c312bcfb0dc01eef67aea0db19e97ee9
Registration Date: August 22, 2022

Manufacturer

Name: VADI Medical Technology Co., Ltd. Yangmei

Authorized Representative

Name: AMTT CO., LTD

About this record

Access comprehensive regulatory information for Humidifier Chamber in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c312bcfb0dc01eef67aea0db19e97ee9 and manufactured by VADI Medical Technology Co., Ltd. Yangmei. The device was registered on August 22, 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.