Taiwan FDA registration c8e927e6528f2785b1629cbb61e263f7

Components for in vitro prosthetics (unsterilized)

TW: "昱康"體外肢體義肢用組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Kenda Road Enterprise Co., Ltd. Xinzhuang Factory;; Yukang Medical Equipment Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
c8e927e6528f2785b1629cbb61e263f7
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Yukang Medical Equipment Co., Ltd
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3420 體外肢體義肢用組件
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
Cancellation Date
Oct 04, 2023
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About this record

Access comprehensive regulatory information for Components for in vitro prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c8e927e6528f2785b1629cbb61e263f7 and manufactured by Kenda Road Enterprise Co., Ltd. Xinzhuang Factory;; Yukang Medical Equipment Co., Ltd. The authorized representative in Taiwan is Yukang Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including NANJING SHULE PROSTHETICS ORTHOTICS LTD, Kenda Road Enterprise Co., Ltd. Xinzhuang Factory, and 5 recent registrations in the same category. 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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