Taiwan FDA registration fd3c0384326856c94172908f56b1809c
“Medi-Tate” iTind System
TW: “邁迪泰特”艾挺得擴張支架
Taiwan·Risk Class 2·MD·Medi-Tate Ltd.·Registered Jan 04, 2023 – Jan 04, 2028ActiveRegistration details
- Analysis ID
- fd3c0384326856c94172908f56b1809c
- License Form
- Ministry of Health Medical Device Import No. 035949
- Customs Code
- DHA05603594900
Company information
- Manufacturer
- Medi-Tate Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- The Medi-Tate Temporary Nitinol Implant Device (iTind) is designed to treat men older than 50 years with lower urinary tract symptoms (LUTS) due to benign prostatic hypertrophy (BPH).
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5520 Urethral dilators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 04, 2023
- Expiry Date
- Jan 04, 2028
About this record
Access comprehensive regulatory information for “Medi-Tate” iTind System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd3c0384326856c94172908f56b1809c and manufactured by Medi-Tate Ltd.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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