Taiwan FDA registration b6c6b02fbf59a19ae7bc4f277e7107d5
"Ginos" percutaneous puncture angioplasty balloon dilation catheter
TW: “吉諾司”經皮穿刺血管成形術球囊擴張導管
Taiwan·Risk Class 2·Genoss Co., Ltd.·Registered Jun 17, 2020 – Jun 17, 2025ExpiredRegistration details
- Analysis ID
- b6c6b02fbf59a19ae7bc4f277e7107d5
- Customs Code
- DHA05603376707
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 Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jun 17, 2020
- Expiry Date
- Jun 17, 2025
About this record
Access comprehensive regulatory information for "Ginos" percutaneous puncture angioplasty balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6c6b02fbf59a19ae7bc4f277e7107d5 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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