"Kindi" medical absorbent fiber (unsterilized) - Taiwan Registration bc927bacbc305ea0e101f5c9d0667ad1
Access comprehensive regulatory information for "Kindi" medical absorbent fiber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bc927bacbc305ea0e101f5c9d0667ad1 and manufactured by HENAN PIAOAN GROUP CO., LTD.. The authorized representative in Taiwan is KING DAY 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.
Device Details
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".
J General hospital and personal use equipment
J.5300 醫療用吸收纖維
Input;; Chinese goods
Dates and Status
Dec 18, 2008
Dec 18, 2018
Jul 15, 2022
Cancellation Information
Logged out
未展延而逾期者