Taiwan FDA registration aaae603f5d325fd89bfb2c23099f6b21
“HONG SHIANG” NEBULIZER
TW: “鴻祥” 噴霧治療器
Taiwan·Risk Class 2·MD·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Oct 18, 2021 – Oct 18, 2026ActiveRegistration details
- Analysis ID
- aaae603f5d325fd89bfb2c23099f6b21
- License Form
- Ministry of Health Medical Device Manufacturing No. 007314
Company information
- Manufacturer
- HONG SHIANG TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HONG SHIANG TECHNOLOGY 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 18, 2021
- Expiry Date
- Oct 18, 2026
About this record
Access comprehensive regulatory information for “HONG SHIANG” NEBULIZER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aaae603f5d325fd89bfb2c23099f6b21 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY 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