Taiwan FDA registration 08131be5de99b15a9f3d47c2d1f39798
“SEAWON” St. Reed Steerable Neurolysis Catheter System
TW: “喜旺”史瑞德活動式硬膜外導管
Taiwan·Risk Class 2·MD·SEAWON MEDITECH CO., LTD.·Registered Jul 29, 2013 – Jul 29, 2023ExpiredRegistration details
- Analysis ID
- 08131be5de99b15a9f3d47c2d1f39798
- License Form
- Ministry of Health Medical Device Import No. 025215
- Customs Code
- DHA05602521501
Company information
- Manufacturer
- SEAWON MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- JUBILANT SUNRISE SCIENTIFIC CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5120 Anesthesia delivery catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2013
- Expiry Date
- Jul 29, 2023
About this record
Access comprehensive regulatory information for “SEAWON” St. Reed Steerable Neurolysis Catheter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 08131be5de99b15a9f3d47c2d1f39798 and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is JUBILANT SUNRISE SCIENTIFIC CO., LTD..
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