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Components for "Changyong" in vitro limb prosthetics (unsterilized) - Taiwan Registration 0e55202478e27b0038ca0153fcedcd29

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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0e55202478e27b0038ca0153fcedcd29
Registration Details
Taiwan FDA Registration: 0e55202478e27b0038ca0153fcedcd29
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Device Details

Components for "Changyong" in vitro limb prosthetics (unsterilized)
TW: "ๅธธๆฐธ"้ซ”ๅค–่‚ข้ซ”็พฉ่‚ข็”จ็ต„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0e55202478e27b0038ca0153fcedcd29

Company Information

Product Details

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.

o Physical Medical Sciences

O.3420 ้ซ”ๅค–่‚ข้ซ”็พฉ่‚ข็”จ็ต„ไปถ

Domestic;; Contract manufacturing

Dates and Status

Mar 16, 2015

Mar 16, 2020

Jun 22, 2022

Cancellation Information

Logged out

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