Taiwan FDA registration 741f200c6afe90d1aee6269c3c83c86e
“FUJIAN PROSTHETICS CENTER”External limb prosthetic component(Non-sterile)
TW: “福建省假肢中心” 體外肢體義肢用組件(未滅菌)
Taiwan·Risk Class 1·MD·FUJIAN PROSTHETICS CENTER·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 741f200c6afe90d1aee6269c3c83c86e
- License Form
- Ministry of Health Medical Device Land Transport Registration No. 001635
- Customs Code
- DHA08600163502
Company information
- Manufacturer
- FUJIAN PROSTHETICS CENTER
- Manufacturer Country
- China
- Authorized Representative
- KEN DALL ENTERPRISE CO., LTD.
Product details
- 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
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for “FUJIAN PROSTHETICS CENTER”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 741f200c6afe90d1aee6269c3c83c86e and manufactured by FUJIAN PROSTHETICS CENTER. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..
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