"CAPRON" Corrective Insole (Non-Sterile)
Taiwan·Risk Class 1·MD·CAPRON PODOLOGIE·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- d014034fe801e3f5c8b3c28a51f929df
- License Form
- Ministry of Health Medical Device Import Registration No. 019701
- Customs Code
- DHA08401970106
- Manufacturer
- CAPRON PODOLOGIE
- Manufacturer Country
- France
- Authorized Representative
- UHEALTH COMPANY LIMITED
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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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 d014034fe801e3f5c8b3c28a51f929df 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.