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“Zeiss” i.Terminal 2 (Non-Sterile) - Taiwan Registration bd3b777eea1b4bf4e93631d3695b83c1

Access comprehensive regulatory information for “Zeiss” i.Terminal 2 (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 bd3b777eea1b4bf4e93631d3695b83c1 and manufactured by CARL ZEISS VISION GMBH. The authorized representative in Taiwan is CARL ZEISS 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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Registration Details
Taiwan FDA Registration: bd3b777eea1b4bf4e93631d3695b83c1
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Device Details

“Zeiss” i.Terminal 2 (Non-Sterile)
TW: “蔡司”瞳孔計 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

bd3b777eea1b4bf4e93631d3695b83c1

Ministry of Health Medical Device Import No. 019456

DHA09401945602

Company Information

Germany

Product Details

M Ophthalmic devices

M1700 Pupillometer

Imported from abroad

Dates and Status

Aug 06, 2018

Aug 06, 2023

Sep 13, 2021

Cancellation Information

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