Taiwan FDA registration 03925e52b6d06bf1305b0d36ad3e7da7
“SEAWON” FORA-B Steerable Epidural Balloon Catheter
TW: “喜旺”佛爾畢可操控硬膜外氣球導管
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Jun 16, 2017 – Jun 16, 2027ActiveRegistration details
- Analysis ID
- 03925e52b6d06bf1305b0d36ad3e7da7
- License Form
- Ministry of Health Medical Device Import No. 029795
- Customs Code
- DHA05602979500
Company information
- Manufacturer
- Seawon Meditech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
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
- Jun 16, 2017
- Expiry Date
- Jun 16, 2027
About this record
Access comprehensive regulatory information for “SEAWON” FORA-B Steerable Epidural Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03925e52b6d06bf1305b0d36ad3e7da7 and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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