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"ZEISS" optotype projector (unsterilized) - Taiwan Registration 94a14c8bd254c0a6bf8dd8b63e9f5769

Access comprehensive regulatory information for "ZEISS" optotype projector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 94a14c8bd254c0a6bf8dd8b63e9f5769 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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94a14c8bd254c0a6bf8dd8b63e9f5769
Registration Details
Taiwan FDA Registration: 94a14c8bd254c0a6bf8dd8b63e9f5769
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Device Details

"ZEISS" optotype projector (unsterilized)
TW: โ€่”กๅธโ€่ฆ–ๆจ™ๆŠ•ๅฝฑๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

94a14c8bd254c0a6bf8dd8b63e9f5769

DHA04400314100

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment (ophthalmic projectors [M.1680]).

M Ophthalmology

M.1680 ็œผ็ง‘็”จๆŠ•ๅฝฑๆฉŸ

import

Dates and Status

Mar 24, 2006

Mar 24, 2016

Nov 16, 2018

Cancellation Information

Logged out

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