Taiwan FDA registration dc70495a825233af1854b71fd84d2025
"Rontes" Knath around the balloon catheter
TW: “朗提仕”克納適周邊氣球導管
Taiwan·Risk Class 2·Rontis Corporation S.A.;; Rontis Hellas S.A.·Registered Oct 21, 2018 – Oct 21, 2023ExpiredRegistration details
- Analysis ID
- dc70495a825233af1854b71fd84d2025
- Customs Code
- DHA05603183004
Company information
- Manufacturer
- Rontis Corporation S.A.;; Rontis Hellas S.A.
- Manufacturer Country
- Greece;;Switzerland
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Oct 21, 2018
- Expiry Date
- Oct 21, 2023
About this record
Access comprehensive regulatory information for "Rontes" Knath around the balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc70495a825233af1854b71fd84d2025 and manufactured by Rontis Corporation S.A.;; Rontis Hellas S.A.. The authorized representative in Taiwan is INTERLINK MEDICAL 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