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“FCI” Ptosis Crutch (Non Sterile) - Taiwan Registration ca10e2062480c125d44b2cee4e5b307c

Access comprehensive regulatory information for “FCI” Ptosis Crutch (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 ca10e2062480c125d44b2cee4e5b307c and manufactured by FCI S.A.S.. The authorized representative in Taiwan is HEALTH CARE MEDICAL INC..

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.

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ca10e2062480c125d44b2cee4e5b307c
Registration Details
Taiwan FDA Registration: ca10e2062480c125d44b2cee4e5b307c
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Device Details

“FCI” Ptosis Crutch (Non Sterile)
TW: “佛朗惜眼” 上眼瞼下垂支持器(未滅菌)
Risk Class 1
MD

Registration Details

ca10e2062480c125d44b2cee4e5b307c

Ministry of Health Medical Device Import No. 022613

DHA09402261302

Company Information

France

Product Details

Limited to the classification and grading management method of medical equipment, the first level identification range of "upper eyelid ptosis supporter (M.5600)".

M Ophthalmic devices

M5600 Upper Eyelid Drosis Supporter

Imported from abroad

Dates and Status

Aug 13, 2021

Aug 13, 2026