Taiwan FDA registration bf1cb023c42c52b8ea18d02e5c75eed0
Kaiwood Luminometer (Non-Sterile)
TW: 開物化學冷光儀 (未滅菌)
Taiwan·Risk Class 1·MD·Kaiwu Technology Co., Ltd. Nanke Factory·Registered Oct 01, 2021 – Oct 31, 2022CancelledRegistration details
- Analysis ID
- bf1cb023c42c52b8ea18d02e5c75eed0
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 001888
- Customs Code
- DHY08300188801
Company information
- Manufacturer
- Kaiwu Technology Co., Ltd. Nanke Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kaiwu Technology Co., Ltd. Nanke Factory
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Kaiwood Luminometer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf1cb023c42c52b8ea18d02e5c75eed0 and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.
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