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"Fubi" OTOLARYNG-throat manual surgical instrument (unsterile) - Taiwan Registration b1d84eff219232294034703fb0644f7b

Access comprehensive regulatory information for "Fubi" OTOLARYNG-throat manual surgical 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 b1d84eff219232294034703fb0644f7b and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, 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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b1d84eff219232294034703fb0644f7b
Registration Details
Taiwan FDA Registration: b1d84eff219232294034703fb0644f7b
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Device Details

"Fubi" OTOLARYNG-throat manual surgical instrument (unsterile)
TW: "ๆ™ฎ็พŽ" ่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b1d84eff219232294034703fb0644f7b

DHA04400309200

Company Information

Germany

Product Details

It is limited to the scope of first-level identification of the Administrative Measures for Medical Devices (Otolaryngology Manual Surgical Instruments [G.4420]).

G ENT Science

G.4420 Otolaryngology manual surgical instruments

import

Dates and Status

Mar 23, 2006

Mar 23, 2011

Jan 18, 2013

Cancellation Information

Logged out

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