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"ZEISS" VISUSCREEN Ophthalmic Projector (non-sterile) - Taiwan Registration cfec2705f00e17052d25183c090f10cf

Access comprehensive regulatory information for "ZEISS" VISUSCREEN Ophthalmic Projector (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 cfec2705f00e17052d25183c090f10cf and manufactured by CARL ZEISS VISION GMBH. The authorized representative in Taiwan is Yakili Corporation of Agili.

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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cfec2705f00e17052d25183c090f10cf
Registration Details
Taiwan FDA Registration: cfec2705f00e17052d25183c090f10cf
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Device Details

"ZEISS" VISUSCREEN Ophthalmic Projector (non-sterile)
TW: "่”กๅธ" ่ฆ–ๆจ™ๆŠ•ๅฝฑๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

cfec2705f00e17052d25183c090f10cf

Ministry of Health Medical Device Import No. 015052

DHA09401505200

Company Information

Germany

Product Details

M Ophthalmic devices

M1680 Ophthalmic Projector

Imported from abroad

Dates and Status

Mar 26, 2015

Mar 26, 2020

Jan 31, 2019

Cancellation Information

Logged out

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