Taiwan FDA registration e69eebf91561b225525ec55d36e8b533
"Blue line" disposable ureteral guide sheath
TW: “藍線”一次性使用輸尿管導引鞘
Taiwan·Risk Class 2·HAIYAN KANGYUAN MEDICAL INSTRUMENT CO., LTD.·Registered Jan 21, 2021 – Jan 21, 2026ExpiredRegistration details
- Analysis ID
- e69eebf91561b225525ec55d36e8b533
- Customs Code
- DHA09200117905
Company information
- Manufacturer
- HAIYAN KANGYUAN MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5130 泌尿導管及其附件
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 21, 2021
- Expiry Date
- Jan 21, 2026
About this record
Access comprehensive regulatory information for "Blue line" disposable ureteral guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e69eebf91561b225525ec55d36e8b533 and manufactured by HAIYAN KANGYUAN MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is REVO LASER CORPORATION.
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