Taiwan FDA registration 76842c1d022fc6c4013af94609632184

“Cheng Chuan”External limb prosthetic component (Non-Sterile)

TW: “正全”體外肢體義肢用組件 (未滅菌)

Taiwan·Risk Class 1·MD·Zhengquan Prosthetic Rehabilitation Equipment Co., Ltd. Taichung Branch·Registered Oct 01, 2021 – Oct 31, 2027Active

Registration details

Analysis ID: 76842c1d022fc6c4013af94609632184
License Form: Ministry of Health Medical Device Manufacturing Registration No. 001758

Company information

Manufacturer: Zhengquan Prosthetic Rehabilitation Equipment Co., Ltd. Taichung Branch
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CHENG CHUAN P&O 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: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2027

About this record

Access comprehensive regulatory information for “Cheng Chuan”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 76842c1d022fc6c4013af94609632184 and manufactured by Zhengquan Prosthetic Rehabilitation Equipment Co., Ltd. Taichung Branch. The authorized representative in Taiwan is CHENG CHUAN P&O CO., LTD..

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