Taiwan FDA registration ca10e2062480c125d44b2cee4e5b307c
“FCI” Ptosis Crutch (Non Sterile)
TW: “佛朗惜眼” 上眼瞼下垂支持器(未滅菌)
Registration details
- Analysis ID
- ca10e2062480c125d44b2cee4e5b307c
- License Form
- Ministry of Health Medical Device Import No. 022613
- Customs Code
- DHA09402261302
Company information
- Manufacturer
- FCI S.A.S.
- Manufacturer Country
- France
- Authorized Representative
- HEALTH CARE MEDICAL INC.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, the first level identification range of "upper eyelid ptosis supporter (M.5600)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5600 Upper Eyelid Drosis Supporter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 13, 2021
- Expiry Date
- Aug 13, 2026
About this record
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..
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