Taiwan FDA registration e9f3bfa977cf1fca86b7cab51a68b49e

"Tesken" plantar pressure tester (unsterilized)

TW: “泰思肯” 足底壓力檢測儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·TEKSCAN INC.·Registered Jul 05, 2021 – Jul 05, 2026Cancelled
Registration details
Analysis ID
e9f3bfa977cf1fca86b7cab51a68b49e
Customs Code
DHA09402257701
Company information
Manufacturer
TEKSCAN INC.
Manufacturer Country
United States
Authorized Representative
MEMS TECHNOLOGY CORP.
Product details
Intended Use
Limited to the first level identification range of the "Force Measuring Board (O.1575)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.1575 Measuring plates
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jul 05, 2021
Expiry Date
Jul 05, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Tesken" plantar pressure tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9f3bfa977cf1fca86b7cab51a68b49e and manufactured by TEKSCAN INC.. The authorized representative in Taiwan is MEMS TECHNOLOGY CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TEKSCAN INC., and 1 recent registrations in the same category. 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.

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