Kaiwood Luminometer (Non-Sterile) - Taiwan Registration bf1cb023c42c52b8ea18d02e5c75eed0
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.
Device Details
Registration Details
bf1cb023c42c52b8ea18d02e5c75eed0
Ministry of Health Medical Device Manufacturing Registration No. 001888
DHY08300188801
Product Details
A Clinical chemistry and clinical toxicology
A2300 Colorimeter, photometer, or spectrophotometer for clinical use
Produced in Taiwan, China
Dates and Status
Oct 01, 2021
Oct 31, 2022
Cancellation Information
Logged out
ๆชๅฑๅปถ่้พๆ่