"Foremount" Space Chamber (Non-Sterile) - Taiwan Registration 48be4c8bee2a56618bb0e09a54f5583e
Access comprehensive regulatory information for "Foremount" Space Chamber (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 48be4c8bee2a56618bb0e09a54f5583e and manufactured by Yuanmao Enterprise Co., Ltd. National Factory. The authorized representative in Taiwan is FOREMOUNT ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
48be4c8bee2a56618bb0e09a54f5583e
Ministry of Health Medical Device Manufacturing No. 006873
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
D Devices for anesthesiology
D5640 Non-respiratory medical nebulizer
Produced in Taiwan, China
Dates and Status
Aug 08, 2017
Aug 08, 2027