Taiwan FDA registration fc6121901afe7e843d791698c5c6b328
“Headstar” Nebulizer Kit and Accessory
TW: “華德”噴霧罐組及配件
Taiwan·Risk Class 2·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Jan 13, 2018 – Jan 13, 2028ActiveRegistration details
- Analysis ID
- fc6121901afe7e843d791698c5c6b328
- License Form
- Ministry of Health Medical Device Manufacturing No. 005970
Company information
- Manufacturer
- HEADSTAR MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEADSTAR MEDICAL PRODUCTS 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
Dates and status
- Registration Date
- Jan 13, 2018
- Expiry Date
- Jan 13, 2028
About this record
Access comprehensive regulatory information for “Headstar” Nebulizer Kit and Accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc6121901afe7e843d791698c5c6b328 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..
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