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"Flex" non-electric living tissue clip (sterilization) - Taiwan Registration 313c392294485e4111e2e5252c55328f

Access comprehensive regulatory information for "Flex" non-electric living tissue clip (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 313c392294485e4111e2e5252c55328f and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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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313c392294485e4111e2e5252c55328f
Registration Details
Taiwan FDA Registration: 313c392294485e4111e2e5252c55328f
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Device Details

"Flex" non-electric living tissue clip (sterilization)
TW: โ€œ็ฆ่Šๅ…‹ๆ–ฏโ€้ž้›ปๅ‹•็š„ๆดป้ซ”็ต„็น”ๅคพ๏ผˆๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

313c392294485e4111e2e5252c55328f

DHA04400884601

Company Information

Product Details

It is limited to the first-level identification scope of the "Gastroenterology-Urology Biological Examination Devices (H.1075)" of the Measures for the Classification and Grading of Medical Devices.

H Gastroenterology and urology

H.1075 ่…ธ่ƒƒ็ง‘-ๆณŒๅฐฟ็ง‘็”Ÿๆชขๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

May 25, 2010

May 25, 2025