Taiwan FDA registration 219747aaa0c339bcf6fd32473d1232ad
Yousheng 3-in-1 spray therapist
TW: 優盛三合一噴霧治療器
Taiwan·Risk Class 2·Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory·Registered Apr 22, 2019 – Apr 22, 2029ActiveRegistration details
- Analysis ID
- 219747aaa0c339bcf6fd32473d1232ad
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROSSMAX INTERNATIONAL LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G Otorhinolaryngology;; D Anesthesiology Science
- Product Type (Level 2)
- D.5630 Aerosols;; G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 22, 2019
- Expiry Date
- Apr 22, 2029
About this record
Access comprehensive regulatory information for Yousheng 3-in-1 spray therapist in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 219747aaa0c339bcf6fd32473d1232ad and manufactured by Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL 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