“KEN DALL” External Limb Prosthetic Component (Non-Sterile)
Taiwan·Risk Class 1·MD·Kenda Road Enterprise Co., Ltd. Xinzhuang Factory·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- 4b000778c66eb502f23b32504c4dd4d1
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 007275
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kenda Road Enterprise Co., Ltd. Xinzhuang Factory
- 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 Equipment for physical medicine
- Product Type (Level 2)
- O3420 Components for in vitro limb prosthetics
- Import Information
- Produced in Taiwan, China
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
Top companies providing products similar to "“KEN DALL” External Limb Prosthetic Component (Non-Sterile)"
Recently registered similar products
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.