Taiwan FDA registration 639fa977be87eb5ce563ec6bf8acdc17

"CAPRON" Corrective Insole (Non-Sterile)

TW: "凱普倫" 矯正鞋墊(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CAPRON PODOLOGIE·Registered Oct 12, 2018 – Oct 12, 2023Cancelled
Registration details
Analysis ID
639fa977be87eb5ce563ec6bf8acdc17
License Form
Ministry of Health Medical Device Import No. 019701
Customs Code
DHA09401970102
Company information
Manufacturer
CAPRON PODOLOGIE
Manufacturer Country
France
Authorized Representative
UHEALTH COMPANY LIMITED
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3475 Body Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 12, 2018
Expiry Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "CAPRON" Corrective 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 639fa977be87eb5ce563ec6bf8acdc17 and manufactured by CAPRON PODOLOGIE. The authorized representative in Taiwan is UHEALTH COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CAPRON PODOLOGIE, 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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