Taiwan FDA registration b5e828155ab5f18c78f957b7e8d6647a
"Kent" medical rubber tubing (unsterilized)
TW: "肯特" 醫療用橡膠管 (未滅菌)
Taiwan·Risk Class 1·KENT ELASTOMER PRODUCTS, INC.·Registered Apr 19, 2006 – Apr 19, 2026ExpiredRegistration details
- Analysis ID
- b5e828155ab5f18c78f957b7e8d6647a
- Customs Code
- DHA04400406808
Company information
- Manufacturer
- KENT ELASTOMER PRODUCTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MIN SHIN INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- import
Dates and status
- Registration Date
- Apr 19, 2006
- Expiry Date
- Apr 19, 2026
About this record
Access comprehensive regulatory information for "Kent" medical rubber tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b5e828155ab5f18c78f957b7e8d6647a and manufactured by KENT ELASTOMER PRODUCTS, INC.. The authorized representative in Taiwan is MIN SHIN INSTRUMENTS 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