Taiwan FDA registration 710e70f831fb04879d4dfafb335b82ee

"Kingyard" Catheter Securement Device (Non-Sterile)

TW: "昆鈺" 導管固定裝置 (未滅菌)

Taiwan·Risk Class 1·MD·KINGYARD TECHNOLOGY CO., LTD.·Registered Sep 27, 2021 – Sep 27, 2026Active

Registration details

Analysis ID: 710e70f831fb04879d4dfafb335b82ee
License Form: Ministry of Health Medical Device Manufacturing No. 009331

Company information

Manufacturer: KINGYARD TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: KINGYARD TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the classification and grading management method of medical equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5210 Endovascular catheter fixation device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Sep 27, 2021
Expiry Date: Sep 27, 2026

About this record

Access comprehensive regulatory information for "Kingyard" Catheter Securement Device (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 710e70f831fb04879d4dfafb335b82ee and manufactured by KINGYARD TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is KINGYARD TECHNOLOGY CO., LTD..

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