Taiwan FDA registration 66aa43c84de53611206e54106622cff0
“Fisher & Paykel” Evaqua2 Infant Breathing Circuits
TW: “費雪派克” 伊娃卡嬰兒呼吸管路
Registration details
- Analysis ID
- 66aa43c84de53611206e54106622cff0
- License Form
- Ministry of Health Medical Device Import No. 034321
- Customs Code
- DHA05603432101
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)
- D5450 Gas humidifier for respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2021
- Expiry Date
- Feb 01, 2026
About this record
Access comprehensive regulatory information for “Fisher & Paykel” Evaqua2 Infant 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 66aa43c84de53611206e54106622cff0 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.
Free DatabasePowered by Pure Global AI89,000+ Devices