Taiwan FDA registration bf301de483433308dfe9a6fc63977cbe

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

TW: “肯達路” 體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Kenda Road Enterprise Co., Ltd. Xinzhuang Factory·Registered May 29, 2018 – May 29, 2023Cancelled
Registration details
Analysis ID
bf301de483433308dfe9a6fc63977cbe
License Form
Ministry of Health Medical Device Manufacturing No. 007275
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3420 Components for in vitro limb prosthetics
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
May 29, 2018
Expiry Date
May 29, 2023
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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