Taiwan FDA registration 7129d6ff4d05f97b70145008fba7f3cc
“BALTON”Valvuloplasty catheter Valver
TW: “拜登”法菲心瓣膜成形導管
Taiwan·Risk Class 2·MD·Balton Sp.z o.o.·Registered Nov 30, 2022 – Nov 30, 2027ActiveRegistration details
- Analysis ID
- 7129d6ff4d05f97b70145008fba7f3cc
- License Form
- Ministry of Health Medical Device Import No. 034629
- Customs Code
- DHA05603462900
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)
- E1255 Aortic valvuloplasty balloon catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 30, 2022
- Expiry Date
- Nov 30, 2027
About this record
Access comprehensive regulatory information for “BALTON”Valvuloplasty catheter Valver in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7129d6ff4d05f97b70145008fba7f3cc and manufactured by Balton Sp.z o.o.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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