Taiwan FDA registration 79933e2ed49a897850e9c0d3c308449f
Balloon catheters around "Rontiles"
TW: “朗提仕”特利通周邊氣球導管
Taiwan·Risk Class 2·Rontis Corporation S.A.;; Rontis Hellas S.A.·Registered Oct 21, 2018 – Oct 21, 2023ExpiredRegistration details
- Analysis ID
- 79933e2ed49a897850e9c0d3c308449f
- Customs Code
- DHA05603182906
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 Balloon catheters around "Rontiles" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79933e2ed49a897850e9c0d3c308449f and manufactured by Rontis Corporation S.A.;; Rontis Hellas S.A.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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