Taiwan FDA registration f8830f15d8607334a1c2e998f46b4c1b
“Genoss” NC GENOSS PTCA Balloon Catheter
TW: “吉諾司” 非順應性冠狀動脈球囊導管
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Dec 07, 2019 – Dec 07, 2024ExpiredRegistration details
- Analysis ID
- f8830f15d8607334a1c2e998f46b4c1b
- License Form
- Ministry of Health Medical Device Import No. 033056
- Customs Code
- DHA05603305600
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2019
- Expiry Date
- Dec 07, 2024
About this record
Access comprehensive regulatory information for “Genoss” NC GENOSS PTCA 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 f8830f15d8607334a1c2e998f46b4c1b and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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