Taiwan FDA registration 48be4c8bee2a56618bb0e09a54f5583e

"Foremount" Space Chamber (Non-Sterile)

TW: "遠貿" 吸藥筒 (未滅菌)

Taiwan·Risk Class 1·MD·Yuanmao Enterprise Co., Ltd. National Factory·Registered Aug 08, 2017 – Aug 08, 2027Active

Registration details

Analysis ID: 48be4c8bee2a56618bb0e09a54f5583e
License Form: Ministry of Health Medical Device Manufacturing No. 006873

Company information

Manufacturer: Yuanmao Enterprise Co., Ltd. National Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FOREMOUNT ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5640 Non-respiratory medical nebulizer
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 08, 2017
Expiry Date: Aug 08, 2027

About this record

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..

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