Taiwan FDA registration fae8a928c86530e883c62f0fe0b600dc
Hyworld sprayer
TW: 合世噴霧器
Taiwan·Risk Class 2·Heshi Biomedical Technology Co., Ltd. Zhonghe Third Factory·Registered Jun 22, 2009 – Jun 22, 2014CancelledRegistration details
- Analysis ID
- fae8a928c86530e883c62f0fe0b600dc
- Customs Code
- DHY00500271507
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEALTH & LIFE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5630 Nebulizer
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 22, 2009
- Expiry Date
- Jun 22, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Hyworld sprayer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fae8a928c86530e883c62f0fe0b600dc and manufactured by Heshi Biomedical Technology Co., Ltd. Zhonghe Third Factory. The authorized representative in Taiwan is HEALTH & LIFE 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