Taiwan FDA registration e1e9aff1f4af35d91785ce1ad8984058
“SEAWON” LIBRA Inflatable Bone Expander System
TW: “喜旺”利普爾椎體骨擴張成型術組
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Nov 10, 2016 – Nov 10, 2021CancelledRegistration details
- Analysis ID
- e1e9aff1f4af35d91785ce1ad8984058
- License Form
- Ministry of Health Medical Device Import No. 029024
- Customs Code
- DHA05602902401
Company information
- Manufacturer
- Seawon Meditech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- JUBILANT SUNRISE SCIENTIFIC CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2016
- Expiry Date
- Nov 10, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “SEAWON” LIBRA Inflatable Bone Expander System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1e9aff1f4af35d91785ce1ad8984058 and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is JUBILANT SUNRISE SCIENTIFIC 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