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"Wissharp" laparoscopic perfusion device - Taiwan Registration 646c18f258b4ace2bca8716767ffddbe

Access comprehensive regulatory information for "Wissharp" laparoscopic perfusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 646c18f258b4ace2bca8716767ffddbe and manufactured by WISAP GESELLCHAFT FรœR WISSENSCHAFTLICHEN APPARATEDAU MBH. The authorized representative in Taiwan is BEAMED 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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646c18f258b4ace2bca8716767ffddbe
Registration Details
Taiwan FDA Registration: 646c18f258b4ace2bca8716767ffddbe
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Device Details

"Wissharp" laparoscopic perfusion device
TW: "ๅจๅคๆ™ฎ"่…น่…”้ก็Œๅ…ฅๅ™จ
Risk Class 2
Cancelled

Registration Details

646c18f258b4ace2bca8716767ffddbe

DHA00601685909

Company Information

Product Details

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

l Obstetrics and Gynecology

L.1730 ่…น่…”้ก็Œๅ…ฅๅ™จ

import

Dates and Status

Jul 11, 2006

Jul 11, 2016

Oct 23, 2015

Cancellation Information

Logged out

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