Taiwan FDA registration 2500ad9623ffff920b6565bc2325b6ab
“Medtronic” NuVent Eustachian Tube Dilation Balloon
TW: “美敦力”紐汎特耳咽管擴張球囊
Taiwan·Risk Class 2·MD·MEDTRONIC XOMED, INC.·Registered Jun 07, 2023 – Jun 07, 2028ActiveRegistration details
- Analysis ID
- 2500ad9623ffff920b6565bc2325b6ab
- License Form
- Ministry of Health Medical Device Import No. 036533
- Customs Code
- DHA05603653300
Company information
- Manufacturer
- MEDTRONIC XOMED, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G4180 Eustachian tube balloon dilation system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 07, 2023
- Expiry Date
- Jun 07, 2028
About this record
Access comprehensive regulatory information for “Medtronic” NuVent Eustachian Tube Dilation Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2500ad9623ffff920b6565bc2325b6ab and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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