Taiwan FDA registration 7ebfab9859e6bb5c299a20daf2b32a37
"Haoyou" guide tube
TW: 〝昊佑〞導引導管
Taiwan·Risk Class 2·Shanghai Kindly Medical Instruments Co., Ltd·Registered Oct 10, 2022 – Oct 10, 2027ActiveRegistration details
- Analysis ID
- 7ebfab9859e6bb5c299a20daf2b32a37
- Customs Code
- DHA09200139103
Company information
- Manufacturer
- Shanghai Kindly Medical Instruments Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- HAO YO ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 10, 2022
- Expiry Date
- Oct 10, 2027
About this record
Access comprehensive regulatory information for "Haoyou" guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7ebfab9859e6bb5c299a20daf2b32a37 and manufactured by Shanghai Kindly Medical Instruments Co., Ltd. The authorized representative in Taiwan is HAO YO ENTERPRISE CO., LTD..
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