Taiwan FDA registration abb0fde2292448de575d2c9bcd5b3a09
"Xinjun" manual emergency respirator
TW: “新駿”手動緊急呼吸器
Taiwan·Risk Class 2·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Aug 07, 2019 – Aug 07, 2024ExpiredRegistration details
- Analysis ID
- abb0fde2292448de575d2c9bcd5b3a09
Company information
- Manufacturer
- HEADSTAR MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- STURDY INDUSTRIAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5915 Hand emergency breathing apparatus
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 07, 2019
- Expiry Date
- Aug 07, 2024
About this record
Access comprehensive regulatory information for "Xinjun" manual emergency respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number abb0fde2292448de575d2c9bcd5b3a09 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is STURDY INDUSTRIAL CO., LTD..
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