Taiwan FDA registration e82fef114d39705b415e6b45b4280920
Microlife Mesh Nebulizer
TW: 百略醫學 網篩式霧化器
Taiwan·Risk Class 2·MD·PU YUAN BIOTECH CO., LTD.·Registered Feb 13, 2018 – Feb 13, 2028ActiveRegistration details
- Analysis ID
- e82fef114d39705b415e6b45b4280920
- License Form
- Ministry of Health Medical Device Manufacturing No. 006056
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
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 13, 2018
- Expiry Date
- Feb 13, 2028
About this record
Access comprehensive regulatory information for Microlife Mesh Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e82fef114d39705b415e6b45b4280920 and manufactured by PU YUAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PU YUAN BIOTECH CO., LTD..
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