Taiwan FDA registration eb5296e4dea2ebfa21f996bc72beefb6
“Fisher&Paykel” SleepStyle CPAP system
TW: “費雪派克”正壓呼吸輔助器
Taiwan·Risk Class 2·MD·FISHER & PAYKEL HEALTHCARE LTD.·Registered Oct 22, 2018 – Oct 22, 2028ActiveRegistration details
- Analysis ID
- eb5296e4dea2ebfa21f996bc72beefb6
- License Form
- Ministry of Health Medical Device Import No. 031831
- Customs Code
- DHA05603183106
Company information
- Manufacturer
- FISHER & PAYKEL HEALTHCARE LTD.
- Manufacturer Country
- New Zealand
- Authorized Representative
- FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND)
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)
- D5905 Discontinuous respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2018
- Expiry Date
- Oct 22, 2028
About this record
Access comprehensive regulatory information for “Fisher&Paykel” SleepStyle CPAP system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eb5296e4dea2ebfa21f996bc72beefb6 and manufactured by FISHER & PAYKEL HEALTHCARE LTD.. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).
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