Taiwan FDA registration 29377f59f379c24bdb9bfcb0f110827a
"Lucy" renal stoma catheter
TW: “路希”腎臟造口導管
Taiwan·Risk Class 2·Teleflex Medical;; ARROW INTERNATIONAL CR A.S.·Registered Jan 10, 2019 – Jan 10, 2029ActiveRegistration details
- Analysis ID
- 29377f59f379c24bdb9bfcb0f110827a
- Customs Code
- DHA05603194001
Company information
- Manufacturer
- Teleflex Medical;; ARROW INTERNATIONAL CR A.S.
- Manufacturer Country
- Ireland;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jan 10, 2019
- Expiry Date
- Jan 10, 2029
About this record
Access comprehensive regulatory information for "Lucy" renal stoma catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29377f59f379c24bdb9bfcb0f110827a and manufactured by Teleflex Medical;; ARROW INTERNATIONAL CR A.S.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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