Taiwan FDA registration 0f608a58b5e2f919497b94a09fac7b1b

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·Registered Apr 15, 2011 – Apr 15, 2026Cancelled
Registration details
Analysis ID
0f608a58b5e2f919497b94a09fac7b1b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Yukang Medical Equipment Co., Ltd
Product details
Intended Use
Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.
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
Contract manufacturing;; Domestic
Dates and status
Registration Date
Apr 15, 2011
Expiry Date
Apr 15, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 0f608a58b5e2f919497b94a09fac7b1b and manufactured by Kenda Road Enterprise Co., Ltd. Xinzhuang Factory. 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 Kenda Road Enterprise Co., Ltd. Xinzhuang Factory;; Yukang Medical Equipment Co., Ltd, NANJING SHULE PROSTHETICS ORTHOTICS LTD, 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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