Taiwan FDA registration 419ae7c7f80931ed7986b787f9cb7479
“Foremount” Nebulizer Kit and Accessory (Non-Sterile)
TW: “遠貿”噴霧罐組及配件(未滅菌)
Taiwan·Risk Class 2·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Jul 02, 2019 – Jul 02, 2024ExpiredRegistration details
- Analysis ID
- 419ae7c7f80931ed7986b787f9cb7479
- License Form
- Ministry of Health Medical Device Manufacturing No. 006439
Company information
- Manufacturer
- HEADSTAR MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FOREMOUNT ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jul 02, 2019
- Expiry Date
- Jul 02, 2024
About this record
Access comprehensive regulatory information for “Foremount” Nebulizer Kit and Accessory (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 419ae7c7f80931ed7986b787f9cb7479 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is FOREMOUNT ENTERPRISE CO., LTD..
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