Taiwan FDA registration a9a4deecb08764f5dd03939d09e2d76b
“Genoss” Extractor Aspiration Catheter
TW: “吉諾司”血栓清除導管
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Jan 10, 2020 – Jan 10, 2025ExpiredRegistration details
- Analysis ID
- a9a4deecb08764f5dd03939d09e2d76b
- License Form
- Ministry of Health Medical Device Import No. 033088
- Customs Code
- DHA05603308800
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)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 10, 2020
- Expiry Date
- Jan 10, 2025
About this record
Access comprehensive regulatory information for “Genoss” Extractor Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9a4deecb08764f5dd03939d09e2d76b and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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