Taiwan FDA registration 7f76d967678b63778650497b8855de6f

"Tekscan" F-Scan Medical insole (Non-Sterile)

TW: "泰思肯" 醫用鞋墊 (未滅菌)

Taiwan·Risk Class 1·MD·TEKSCAN, INC.·Registered Jul 22, 2015 – Jul 22, 2025Expired

Registration details

Analysis ID: 7f76d967678b63778650497b8855de6f
License Form: Ministry of Health Medical Device Import No. 015494
Customs Code: DHA09401549403

Company information

Manufacturer: TEKSCAN, INC.
Manufacturer Country: United States
Authorized Representative: MEMS TECHNOLOGY CORP.

Product details

Intended Use: Limited to the first level identification scope of "Medical Insoles (J.6280)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6280 Medical insole
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 22, 2015
Expiry Date: Jul 22, 2025

About this record

Access comprehensive regulatory information for "Tekscan" F-Scan Medical insole (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 7f76d967678b63778650497b8855de6f and manufactured by TEKSCAN, INC.. The authorized representative in Taiwan is MEMS TECHNOLOGY CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.