Taiwan FDA registration 69b31b9ce2dc7a50ae82809a2cb4f72d
"Shisei" medical gauze (unsterilized)
TW: "資生" 醫用紗布 (未滅菌)
Taiwan·Risk Class 1·HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD·Registered Oct 11, 2012 – Oct 11, 2027ActiveRegistration details
- Analysis ID
- 69b31b9ce2dc7a50ae82809a2cb4f72d
- Customs Code
- DHA04600176709
Company information
- Manufacturer Country
- China
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
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
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 11, 2012
- Expiry Date
- Oct 11, 2027
About this record
Access comprehensive regulatory information for "Shisei" medical gauze (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 69b31b9ce2dc7a50ae82809a2cb4f72d and manufactured by HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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