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“KEN DALL” External Limb Prosthetic Component (Non-Sterile) - Taiwan Registration 4b000778c66eb502f23b32504c4dd4d1

Access comprehensive regulatory information for “KEN DALL” External Limb Prosthetic Component (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4b000778c66eb502f23b32504c4dd4d1 and manufactured by Kenda Road Enterprise Co., Ltd. Xinzhuang Factory. The authorized representative in Taiwan is Kenda Road Enterprise Co., Ltd. Xinzhuang Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Kenda Road Enterprise Co., Ltd. Xinzhuang Factory, and 1 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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4b000778c66eb502f23b32504c4dd4d1
Registration Details
Taiwan FDA Registration: 4b000778c66eb502f23b32504c4dd4d1
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Device Details

“KEN DALL” External Limb Prosthetic Component (Non-Sterile)
TW: “肯達路” 體外肢體義肢用組件 (未滅菌)
Risk Class 1
MD

Registration Details

4b000778c66eb502f23b32504c4dd4d1

Ministry of Health Medical Device Manufacturing Registration No. 007275

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 Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2023

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