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“Medi-Tate” iTind System - Taiwan Registration fd3c0384326856c94172908f56b1809c

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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fd3c0384326856c94172908f56b1809c
Registration Details
Taiwan FDA Registration: fd3c0384326856c94172908f56b1809c
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Device Details

“Medi-Tate” iTind System
TW: “邁迪泰特”艾挺得擴張支架
Risk Class 2
MD

Registration Details

fd3c0384326856c94172908f56b1809c

Ministry of Health Medical Device Import No. 035949

DHA05603594900

Company Information

Israel

Product Details

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).

H Gastroenterology and urology

H5520 Urethral dilators

Imported from abroad

Dates and Status

Jan 04, 2023

Jan 04, 2028