Taiwan FDA registration f3113f4c1c3dd5f086240acdda381752
“Genoss” Initiator Angiographic Catheter
TW: “吉諾司”血管攝影導管
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Nov 29, 2019 – Nov 29, 2024ExpiredRegistration details
- Analysis ID
- f3113f4c1c3dd5f086240acdda381752
- License Form
- Ministry of Health Medical Device Import No. 033048
- Customs Code
- DHA05603304801
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)
- E1200 Diagnostic endovascular catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 29, 2019
- Expiry Date
- Nov 29, 2024
About this record
Access comprehensive regulatory information for “Genoss” Initiator Angiographic Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3113f4c1c3dd5f086240acdda381752 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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