Taiwan FDA registration 03dcacb0b155781e98c4f943f150b3a5
“Fisher & Paykel” High Flow Heated Respiratory Humidifier
TW: “費雪派克”高流量加熱式呼吸加濕器
Taiwan·Risk Class 2·MD·FISHER & PAYKEL HEALTHCARE LIMITED·Registered Nov 24, 2016 – Nov 24, 2026ActiveRegistration details
- Analysis ID
- 03dcacb0b155781e98c4f943f150b3a5
- License Form
- Ministry of Health Medical Device Import No. 029121
- Customs Code
- DHA05602912109
Company information
- Manufacturer
- FISHER & PAYKEL HEALTHCARE LIMITED
- 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)
- D5450 Gas humidifier for respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 24, 2016
- Expiry Date
- Nov 24, 2026
About this record
Access comprehensive regulatory information for “Fisher & Paykel” High Flow Heated Respiratory Humidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03dcacb0b155781e98c4f943f150b3a5 and manufactured by FISHER & PAYKEL HEALTHCARE LIMITED. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).
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