Taiwan FDA registration cbe7c8f524bcdbdb66cd9fb1c0a6dcfc
“Maxtec” Air/Oxygen Blender
TW: “麥斯特克” 空氣/氧氣混合器
Taiwan·Risk Class 2·MD·MAXTEC, LLC·Registered Oct 18, 2021 – Oct 18, 2026ActiveRegistration details
- Analysis ID
- cbe7c8f524bcdbdb66cd9fb1c0a6dcfc
- License Form
- Ministry of Health Medical Device Import No. 034879
- Customs Code
- DHA05603487900
Company information
- Manufacturer
- MAXTEC, LLC
- Manufacturer Country
- United States
- 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 Devices for anesthesiology
- Product Type (Level 2)
- D5330 Breathing Gas Mixer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 18, 2021
- Expiry Date
- Oct 18, 2026
About this record
Access comprehensive regulatory information for “Maxtec” Air/Oxygen Blender in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cbe7c8f524bcdbdb66cd9fb1c0a6dcfc and manufactured by MAXTEC, LLC. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).
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