Taiwan FDA registration b6ce2b3d03fa13a806c10ef5ea084a8b
“SEAWON” FORA-B TF Transforaminal Epidural Balloon Catheter System
TW: “喜旺”佛爾畢經椎間孔硬膜外球囊導管組
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Dec 26, 2019 – Dec 26, 2024ExpiredRegistration details
- Analysis ID
- b6ce2b3d03fa13a806c10ef5ea084a8b
- License Form
- Ministry of Health Medical Device Import No. 033077
- Customs Code
- DHA05603307708
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
- Dec 26, 2019
- Expiry Date
- Dec 26, 2024
About this record
Access comprehensive regulatory information for “SEAWON” FORA-B TF Transforaminal Epidural Balloon 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 b6ce2b3d03fa13a806c10ef5ea084a8b and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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