Taiwan FDA registration 7ea7b0807cf9af062af3af63e6b4ecc5

Components for in vitro prosthetics (unsterilized)

TW: “肯達路”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 Aug 03, 2006 – Aug 03, 2021Cancelled
Registration details
Analysis ID
7ea7b0807cf9af062af3af63e6b4ecc5
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
Dates and status
Registration Date
Aug 03, 2006
Expiry Date
Aug 03, 2021
Cancellation Date
Aug 29, 2018
Cancellation information
Status
Logged out
Reason
工廠歇業
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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 7ea7b0807cf9af062af3af63e6b4ecc5 and manufactured by The second plant of Kenda Road Enterprise Co., Ltd. The authorized representative in Taiwan is The second plant of Kenda Road Enterprise 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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