Taiwan FDA registration 0e55202478e27b0038ca0153fcedcd29

Components for "Changyong" in vitro limb prosthetics (unsterilized)

TW: "常永"體外肢體義肢用組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·The second plant of Kenda Road Enterprise Co., Ltd·Registered Mar 16, 2015 – Mar 16, 2020Cancelled
Registration details
Analysis ID
0e55202478e27b0038ca0153fcedcd29
Company information
Manufacturer Country
Taiwan, Province of China
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
Domestic;; Contract manufacturing
Dates and status
Registration Date
Mar 16, 2015
Expiry Date
Mar 16, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Components for "Changyong" in vitro limb 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 0e55202478e27b0038ca0153fcedcd29 and manufactured by The second plant of Kenda Road Enterprise Co., Ltd. The authorized representative in Taiwan is Changyong Prosthetic Assistive Devices Co., Ltd.

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