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"Fidia" Al vitreous replacement - Taiwan Registration c41960f84af1c611fa705024b8ee44dc

Access comprehensive regulatory information for "Fidia" Al vitreous replacement in Taiwan's medical device market through Pure Global AI's free database. is registered under number c41960f84af1c611fa705024b8ee44dc and manufactured by FIDIA FARMACEUTICI S.P.A.. The authorized representative in Taiwan is MED PHARMA CO., LTD..

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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c41960f84af1c611fa705024b8ee44dc
Registration Details
Taiwan FDA Registration: c41960f84af1c611fa705024b8ee44dc
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Device Details

"Fidia" Al vitreous replacement
TW: "่ฒ่ฟช้›…" ่‰พ็ˆพ็Žป็’ƒ้ซ”ๆ›ฟไปฃ็‰ฉ
Cancelled

Registration Details

c41960f84af1c611fa705024b8ee44dc

DHA00600980903

Company Information

Italy

Product Details

Suitable for use in anterior or posterior chamber surgery and removed before surgery is completed.

M Ophthalmology

import

Dates and Status

Jan 18, 2002

Jan 18, 2007

Nov 09, 2012

Cancellation Information

Logged out

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