Taiwan FDA registration 167ef08048f8005143c4340ece12098d
"K.F." Cane (Non-Sterile)
TW: "康復" 手杖 (未滅菌)
Registration details
- Analysis ID
- 167ef08048f8005143c4340ece12098d
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 003619
Company information
- Manufacturer
- CHANG CHENG FA ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PUN LEAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Medical Cane (O.3075)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3075 Medical cane
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "K.F." Cane (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 167ef08048f8005143c4340ece12098d and manufactured by CHANG CHENG FA ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PUN LEAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices