"Kindi" medical absorbent fiber (unsterilized)
Taiwan·Risk Class 1·HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.·Registered Nov 27, 2012 – Nov 27, 2027Active- Analysis ID
- ec9ce5297492cec14dcef6f0ed149661
- Customs Code
- DHA04600179807
- Manufacturer Country
- China
- Authorized Representative
- KING DAY CO., LTD.
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Medical Absorbent Fiber (J.5300) First Grade Identification Range".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5300 醫療用吸收纖維
- Import Information
- Input;; Chinese goods
- Registration Date
- Nov 27, 2012
- Expiry Date
- Nov 27, 2027
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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.