Taiwan FDA registration a4f84c9cacbb5283c202c57591a8f033
“Seawon” SIMC Steerable Neurolysis Cervical Catheter
TW: “希旺”可導引式脊椎手術套組
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Dec 16, 2021 – Dec 16, 2026ActiveRegistration details
- Analysis ID
- a4f84c9cacbb5283c202c57591a8f033
- License Form
- Ministry of Health Medical Device Import No. 035116
- Customs Code
- DHA05603511602
Company information
- Manufacturer
- Seawon Meditech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5120 Anesthesia delivery catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2021
- Expiry Date
- Dec 16, 2026
About this record
Access comprehensive regulatory information for “Seawon” SIMC Steerable Neurolysis Cervical Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4f84c9cacbb5283c202c57591a8f033 and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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