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"Du Ke" manual ophthalmic surgery instrument (unsterile) - Taiwan Registration 1129eb9f589c3b073974fecca3da37dd

Access comprehensive regulatory information for "Du Ke" manual ophthalmic surgery instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1129eb9f589c3b073974fecca3da37dd and manufactured by DUCKWORTH & KENT LTD. The authorized representative in Taiwan is BIO-LIFE ENTERPRISE 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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1129eb9f589c3b073974fecca3da37dd
Registration Details
Taiwan FDA Registration: 1129eb9f589c3b073974fecca3da37dd
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Device Details

"Du Ke" manual ophthalmic surgery instrument (unsterile)
TW: "ๆœๅ…‹" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1129eb9f589c3b073974fecca3da37dd

DHA04400387101

Company Information

United Kingdom

Product Details

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Apr 14, 2006

Apr 14, 2011

Aug 01, 2011

Cancellation Information

Logged out

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