Taiwan FDA registration 9121a12297dfeaf155a939d5997dc9d0

"TIDI" Intravascular catheter securement device (Non-Sterile)

TW: "迪艾迪艾" 血管內導管固定裝置 (未滅菌)

Taiwan·Risk Class 1·MD·TIDI PRODUCTS, LLC·Registered Sep 12, 2017 – Sep 12, 2022Expired

Registration details

Analysis ID: 9121a12297dfeaf155a939d5997dc9d0
License Form: Ministry of Health Medical Device Import No. 018301
Customs Code: DHA09401830107

Company information

Manufacturer: TIDI PRODUCTS, LLC
Manufacturer Country: United States
Authorized Representative: FRIENDS SCIENTIFIC CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5210 Endovascular catheter fixation device
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 12, 2017
Expiry Date: Sep 12, 2022

About this record

Access comprehensive regulatory information for "TIDI" Intravascular 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 9121a12297dfeaf155a939d5997dc9d0 and manufactured by TIDI PRODUCTS, LLC. The authorized representative in Taiwan is FRIENDS SCIENTIFIC CO., LTD..

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