Taiwan FDA registration 5eaaa15cc212f46aa760278d69fb4928
"Crown" sputum tube (pack) (sterilization)
TW: "皇冠" 抽痰管 (包) (滅菌)
Taiwan·Risk Class 1·ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.·Registered Mar 31, 2006 – Mar 31, 2026ExpiredRegistration details
- Analysis ID
- 5eaaa15cc212f46aa760278d69fb4928
- Customs Code
- DHA04600015601
Company information
- Manufacturer Country
- China
- Authorized Representative
- LAIFA CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 31, 2006
- Expiry Date
- Mar 31, 2026
About this record
Access comprehensive regulatory information for "Crown" sputum tube (pack) (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5eaaa15cc212f46aa760278d69fb4928 and manufactured by ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is LAIFA 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