Taiwan FDA registration ba3c26994495b33dd20419c3a35c9a50
“Pu Yuan”Accurate Portable Nebulizer
TW: “普元”艾可瑞攜帶式噴霧器
Taiwan·Risk Class 2·MD·PU YUAN BIOTECH CO., LTD.·Registered Jan 30, 2023 – Jan 30, 2028ActiveRegistration details
- Analysis ID
- ba3c26994495b33dd20419c3a35c9a50
- License Form
- Ministry of Health Medical Device Manufacturing No. 007798
Company information
- Manufacturer
- PU YUAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PU YUAN BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 30, 2023
- Expiry Date
- Jan 30, 2028
About this record
Access comprehensive regulatory information for “Pu Yuan”Accurate Portable Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba3c26994495b33dd20419c3a35c9a50 and manufactured by PU YUAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PU YUAN BIOTECH CO., LTD..
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