Taiwan FDA registration 511bc36cda448796950f07f9d0785daf
“BALTON”River CTO Coronary Angioplasty Cathether
TW: “拜登”羅凡賽冠狀動脈慢性阻塞擴張導管
Taiwan·Risk Class 2·MD·Balton Sp.z o.o.·Registered Oct 03, 2022 – Oct 03, 2027ActiveRegistration details
- Analysis ID
- 511bc36cda448796950f07f9d0785daf
- License Form
- Ministry of Health Medical Device Import No. 034624
- Customs Code
- DHA05603462403
Company information
- Manufacturer
- Balton Sp.z o.o.
- Manufacturer Country
- Poland
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2022
- Expiry Date
- Oct 03, 2027
About this record
Access comprehensive regulatory information for “BALTON”River CTO Coronary Angioplasty Cathether in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 511bc36cda448796950f07f9d0785daf and manufactured by Balton Sp.z o.o.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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