Taiwan FDA registration bfa6cb5915149a7cc5e5fc52695bafd4
"Mu Kang" small molecule portable sprayer
TW: “慕康” 小分子攜帶式噴霧器
Registration details
- Analysis ID
- bfa6cb5915149a7cc5e5fc52695bafd4
Company information
- Manufacturer
- PU YUAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Mediera Corporation
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5630 Nebulizer
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Nov 22, 2021
- Expiry Date
- May 15, 2029
About this record
Access comprehensive regulatory information for "Mu Kang" small molecule portable sprayer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfa6cb5915149a7cc5e5fc52695bafd4 and manufactured by PU YUAN BIOTECH CO., LTD.. The authorized representative in Taiwan is Mediera Corporation.
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