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"Metifix" non-powered neurosurgical instruments (unsterilized) - Taiwan Registration a3faa0b6537852a575006fda1d230d67

Access comprehensive regulatory information for "Metifix" non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a3faa0b6537852a575006fda1d230d67 and manufactured by MEDIFLEX DIVISION OF FLEXBAR MACHINE CORPORATION. The authorized representative in Taiwan is Liren Equipment Factory 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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a3faa0b6537852a575006fda1d230d67
Registration Details
Taiwan FDA Registration: a3faa0b6537852a575006fda1d230d67
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Device Details

"Metifix" non-powered neurosurgical instruments (unsterilized)
TW: "ๆข…ๅธ่ฒๅ…‹ๆ–ฏ" ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a3faa0b6537852a575006fda1d230d67

DHA04400388305

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".

K Neuroscience

K.4535 ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ

import

Dates and Status

Apr 14, 2006

Apr 14, 2021

Sep 23, 2023

Cancellation Information

Logged out

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