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"Flex" Gastroenterology-Urology Bioexamination Equipment (Sterilized/Unsterilized) - Taiwan Registration d74ffe54e0dc02617a9e2a5ccb528362

Access comprehensive regulatory information for "Flex" Gastroenterology-Urology Bioexamination Equipment (Sterilized/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d74ffe54e0dc02617a9e2a5ccb528362 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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d74ffe54e0dc02617a9e2a5ccb528362
Registration Details
Taiwan FDA Registration: d74ffe54e0dc02617a9e2a5ccb528362
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Device Details

"Flex" Gastroenterology-Urology Bioexamination Equipment (Sterilized/Unsterilized)
TW: "็ฆ่Šๅ…‹ๆ–ฏ" ่…ธ่ƒƒ็ง‘-ๆณŒๅฐฟ็ง‘็”Ÿๆชขๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d74ffe54e0dc02617a9e2a5ccb528362

DHA09401626608

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 16, 2016

Mar 16, 2026