Taiwan FDA registration f3f6aa38055c82e019a78026c7bd5043
Ruikang glucose solution (unsterilized)
TW: 瑞康 葡萄糖品管液 (未滅菌)
Taiwan·Risk Class 1·Heshi Biomedical Technology Co., Ltd. Zhonghe No. 2 Factory·Registered May 07, 2013 – May 07, 2018CancelledRegistration details
- Analysis ID
- f3f6aa38055c82e019a78026c7bd5043
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEALTH & LIFE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- May 07, 2013
- Expiry Date
- May 07, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ruikang glucose solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f3f6aa38055c82e019a78026c7bd5043 and manufactured by Heshi Biomedical Technology Co., Ltd. Zhonghe No. 2 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