Taiwan FDA registration 824eaa4dc700a9b0cf17437719b08262
"Jeti" disposable lead-in/drainage catheter (sterilized)
TW: “捷蒂”拋棄式導入/引流導管 (滅菌)
Taiwan·Risk Class 1·JEIL TECH CO., LTD.·Registered Dec 23, 2013 – Dec 23, 2018CancelledRegistration details
- Analysis ID
- 824eaa4dc700a9b0cf17437719b08262
- Customs Code
- DHA09401370802
Company information
- Manufacturer
- JEIL TECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Chengyou An Technology Co., Ltd
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4200 Incoming/Drainage Tubes and Accessories
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 23, 2013
- Expiry Date
- Dec 23, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Jeti" disposable lead-in/drainage catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 824eaa4dc700a9b0cf17437719b08262 and manufactured by JEIL TECH CO., LTD.. The authorized representative in Taiwan is Chengyou An Technology Co., Ltd.
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