Taiwan FDA registration 0bd78afa4ae1d5b80cddefb576ae15de
F&P 950 breathing humidity heater system
TW: “費雪派克” F&P 950呼吸潮濕加熱器系統
Taiwan·Risk Class 2·Fisher & Paykel Healthcare Ltd.·Registered Oct 10, 2023 – Oct 10, 2028ActiveRegistration details
- Analysis ID
- 0bd78afa4ae1d5b80cddefb576ae15de
- Customs Code
- DHA05603662604
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)
- D.5450 Vapor moisture apparatus for respirators
- Import Information
- import
Dates and status
- Registration Date
- Oct 10, 2023
- Expiry Date
- Oct 10, 2028
About this record
Access comprehensive regulatory information for F&P 950 breathing humidity heater system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0bd78afa4ae1d5b80cddefb576ae15de and manufactured by Fisher & Paykel Healthcare Ltd.. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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