Taiwan FDA registration e0b53d9c1243d6e2d0c9a05a02094fbb
“Headstar” Anesthesia Breathing Circuit (Non-sterile)
TW: “華德”麻醉呼吸管路(未滅菌)
Taiwan·Risk Class 1·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Jan 24, 2019 – Jan 24, 2024ExpiredRegistration details
- Analysis ID
- e0b53d9c1243d6e2d0c9a05a02094fbb
- License Form
- Ministry of Health Medical Device Manufacturing No. 007633
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
- Limited to the first level identification range of the "anesthesia breathing circuit (D.5240)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5240 Anesthesia breathing line
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 24, 2019
- Expiry Date
- Jan 24, 2024
About this record
Access comprehensive regulatory information for “Headstar” Anesthesia Breathing Circuit (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 e0b53d9c1243d6e2d0c9a05a02094fbb and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..
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