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“KEN DALL” External Limb Prosthetic Component (Non-Sterile) - Taiwan Registration bf301de483433308dfe9a6fc63977cbe

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 bf301de483433308dfe9a6fc63977cbe 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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bf301de483433308dfe9a6fc63977cbe
Registration Details
Taiwan FDA Registration: bf301de483433308dfe9a6fc63977cbe
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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
Cancelled

Registration Details

bf301de483433308dfe9a6fc63977cbe

Ministry of Health Medical Device Manufacturing No. 007275

Company Information

Product Details

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Produced in Taiwan, China

Dates and Status

May 29, 2018

May 29, 2023

Cancellation Information

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