Taiwan FDA registration 8aa05b75cc97b4d662711d581ebcf481
Respitronics Elite Nebulization Therapy System
TW: 依力特霧化治療系統
Taiwan·Risk Class 2·MD·PU YUAN BIOTECH CO., LTD.·Registered Oct 07, 2021 – Oct 07, 2026ActiveRegistration details
- Analysis ID
- 8aa05b75cc97b4d662711d581ebcf481
- License Form
- Ministry of Health Medical Device Manufacturing No. 007311
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 Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 07, 2021
- Expiry Date
- Oct 07, 2026
About this record
Access comprehensive regulatory information for Respitronics Elite Nebulization Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8aa05b75cc97b4d662711d581ebcf481 and manufactured by PU YUAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PU YUAN BIOTECH CO., LTD..
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