Taiwan FDA registration 481f817d045a8723906c046d8c41b4b0

"WanDer" External Limb Prosthetic Component (Non-Sterile)

TW: "萬德" 體外肢體義肢用組件 (未滅菌)

Taiwan·Risk Class 1·MD·Wande Disabled Equipment Co., Ltd. Zhonghe Factory·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: 481f817d045a8723906c046d8c41b4b0
License Form: Ministry of Health Medical Device Manufacturing Registration No. 005648

Company information

Manufacturer: Wande Disabled Equipment Co., Ltd. Zhonghe Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WAN DER DIABLED PERSON'S AID & SUPPLIES. 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, 2025

About this record

Access comprehensive regulatory information for "WanDer" 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 481f817d045a8723906c046d8c41b4b0 and manufactured by Wande Disabled Equipment Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is WAN DER DIABLED PERSON'S AID & SUPPLIES. CO., LTD..

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