Taiwan FDA registration 1f9f0ce061717300a7c735ce0d50bca9
"Hongjie" gauze (sterilized/unsterilized)
TW: "泓傑" 紗布 (滅菌/未滅菌)
Registration details
- Analysis ID
- 1f9f0ce061717300a7c735ce0d50bca9
Company information
- Manufacturer
- HONG JIER ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HONG JIER ENTERPRISE CO., LTD.
Product details
- 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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Oct 17, 2011
- Expiry Date
- Oct 17, 2026
About this record
Access comprehensive regulatory information for "Hongjie" gauze (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f9f0ce061717300a7c735ce0d50bca9 and manufactured by HONG JIER ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HONG JIER ENTERPRISE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices