"Kindi" medical absorbent fiber (unsterilized) - Taiwan Registration ec9ce5297492cec14dcef6f0ed149661
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 ec9ce5297492cec14dcef6f0ed149661 and manufactured by HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is KING DAY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HENAN PIAOAN GROUP CO., LTD., and 1 recent registrations in the same category. 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 classification and grading management measures of medical equipment "Medical Absorbent Fiber (J.5300) First Grade Identification Range".
J General hospital and personal use equipment
J.5300 ้ซ็็จๅธๆถ็บ็ถญ
Input;; Chinese goods
Dates and Status
Nov 27, 2012
Nov 27, 2027