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"Rudolph" laparoscopic perfusion device (unsterilized) - Taiwan Registration 62c9b5af7b11af383a2335df0c5707b1

Access comprehensive regulatory information for "Rudolph" laparoscopic perfusion device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 62c9b5af7b11af383a2335df0c5707b1 and manufactured by RUDOLF MEDICAL GMBH + CO. KG. The authorized representative in Taiwan is EVERMED INTERNATIONAL 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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62c9b5af7b11af383a2335df0c5707b1
Registration Details
Taiwan FDA Registration: 62c9b5af7b11af383a2335df0c5707b1
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Device Details

"Rudolph" laparoscopic perfusion device (unsterilized)
TW: โ€œ้ญฏ้“ๅคซโ€ ่…น่…”้ก็Œๅ…ฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

62c9b5af7b11af383a2335df0c5707b1

DHA04401216107

Company Information

Germany

Product Details

Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.

l Obstetrics and Gynecology

L.1730 ่…น่…”้ก็Œๅ…ฅๅ™จ

import

Dates and Status

Sep 14, 2012

Sep 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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