Taiwan FDA registration eace411f6503b9ed53a49483be688750
“Fisher & Paykel” Adult Heated Breathing Circuits
TW: “費雪派克” 成人加熱呼吸管路
Taiwan·Risk Class 2·MD·Fisher & Paykel Healthcare Ltd.·Registered Aug 21, 2023 – Aug 21, 2028ActiveRegistration details
- Analysis ID
- eace411f6503b9ed53a49483be688750
- License Form
- Ministry of Health Medical Device Import No. 036586
- Customs Code
- DHA05603658605
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
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5450 Gas humidifier for respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 21, 2023
- Expiry Date
- Aug 21, 2028
About this record
Access comprehensive regulatory information for “Fisher & Paykel” Adult Heated Breathing Circuits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eace411f6503b9ed53a49483be688750 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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