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"Gleich" general manual instruments for obstetrics and gynecology and their accessories (unsterilized) - Taiwan Registration 30bbd01ea18b42d2548217867d988323

Access comprehensive regulatory information for "Gleich" general manual instruments for obstetrics and gynecology and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30bbd01ea18b42d2548217867d988323 and manufactured by QURESHI MANUFACTURING CORPORATION. The authorized representative in Taiwan is AK INSTRUMENTS 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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30bbd01ea18b42d2548217867d988323
Registration Details
Taiwan FDA Registration: 30bbd01ea18b42d2548217867d988323
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Device Details

"Gleich" general manual instruments for obstetrics and gynecology and their accessories (unsterilized)
TW: "ๆ ผๅˆฉๅธŒ" ๅฉฆ็”ข็ง‘็”จไธ€่ˆฌๆ‰‹ๅ‹•ๅ™จๆขฐๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

30bbd01ea18b42d2548217867d988323

DHA04400391900

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".

l Obstetrics and Gynecology

L.4520 ๅฉฆ็”ข็ง‘็”จไธ€่ˆฌๆ‰‹ๅ‹•ๅ™จๆขฐ

import

Dates and Status

Apr 14, 2006

Apr 14, 2016

Aug 14, 2018

Cancellation Information

Logged out

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