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"FCI" Ptosis Curtch (Non-Sterile) - Taiwan Registration 116e0c70ca50f6ea64bc3c1a35ef948c

Access comprehensive regulatory information for "FCI" Ptosis Curtch (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 116e0c70ca50f6ea64bc3c1a35ef948c and manufactured by FCI SAS. 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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116e0c70ca50f6ea64bc3c1a35ef948c
Registration Details
Taiwan FDA Registration: 116e0c70ca50f6ea64bc3c1a35ef948c
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Device Details

"FCI" Ptosis Curtch (Non-Sterile)
TW: "ไฝ›ๆœ—ๆƒœ็œผ" ไธŠ็œผ็žผไธ‹ๅž‚ๆ”ฏๆŒๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

116e0c70ca50f6ea64bc3c1a35ef948c

Ministry of Health Medical Device Import No. 015569

DHA09401556908

Company Information

France

Product Details

M Ophthalmic devices

M5600 Upper Eyelid Drosis Supporter

Imported from abroad

Dates and Status

Aug 11, 2015

Aug 11, 2020

Jun 22, 2022

Cancellation Information

Logged out

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