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"Pademk" neurostimulator - Taiwan Registration 00a8fe662d791427ad7229a602b369ed

Access comprehensive regulatory information for "Pademk" neurostimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00a8fe662d791427ad7229a602b369ed and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong 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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00a8fe662d791427ad7229a602b369ed
Registration Details
Taiwan FDA Registration: 00a8fe662d791427ad7229a602b369ed
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Device Details

"Pademk" neurostimulator
TW: โ€œๅธ•ๅฐ‡ๅ…‹โ€็ฅž็ถ“ๅˆบๆฟ€ๅ™จ
Risk Class 2
Cancelled

Registration Details

00a8fe662d791427ad7229a602b369ed

DHA00602398301

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.2775 Electronic peripheral nerve stimulator

import

Dates and Status

Oct 05, 2012

Oct 05, 2017

Dec 13, 2019

Cancellation Information

Logged out

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