Taiwan FDA registration d74ffe54e0dc02617a9e2a5ccb528362

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

TW: "福萊克斯" 腸胃科-泌尿科生檢器械 (滅菌/未滅菌)
Taiwan flagTaiwan·Risk Class 1·ENDO-FLEX GmbH·Registered Mar 16, 2016 – Mar 16, 2026Expired
Registration details
Analysis ID
d74ffe54e0dc02617a9e2a5ccb528362
Customs Code
DHA09401626608
Company information
Manufacturer
ENDO-FLEX GmbH
Manufacturer Country
Germany
Product details
Intended Use
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.
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1075 腸胃科-泌尿科生檢器械
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Mar 16, 2016
Expiry Date
Mar 16, 2026
About this record

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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