Taiwan FDA registration ededaaa9f773a25eb7edb5b5d8b76904
"Carefusion" Ventilator tubing (Non-Sterile)
TW: "卡爾費"呼吸器管路(未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION·Registered Feb 12, 2018 – Feb 12, 2023ExpiredRegistration details
- Analysis ID
- ededaaa9f773a25eb7edb5b5d8b76904
- License Form
- Ministry of Health Medical Device Import No. 018816
- Customs Code
- DHA09401881601
Company information
- Manufacturer
- CAREFUSION
- Manufacturer Country
- Mexico
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5975 Respirator tubing
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 12, 2018
- Expiry Date
- Feb 12, 2023
About this record
Access comprehensive regulatory information for "Carefusion" Ventilator tubing (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 ededaaa9f773a25eb7edb5b5d8b76904 and manufactured by CAREFUSION. The authorized representative in Taiwan is BIOSYSTEMS INC..
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