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Clinical Template (Sterilization)  - Taiwan Registration fba56ed4afd48aaef04372b486e4b045

Access comprehensive regulatory information for Clinical Template (Sterilization)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fba56ed4afd48aaef04372b486e4b045 and manufactured by MONDEAL MEDICAL SYSTEMS GMBH. The authorized representative in Taiwan is Mengxi Limited.

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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fba56ed4afd48aaef04372b486e4b045
Registration Details
Taiwan FDA Registration: fba56ed4afd48aaef04372b486e4b045
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Device Details

Clinical Template (Sterilization) 
TW: "蒙締邇" 臨床用樣板 (滅菌) 
Risk Class 1
Cancelled

Registration Details

fba56ed4afd48aaef04372b486e4b045

DHA04401205202

Company Information

Germany

Product Details

Limited to the first level identification range of the "clinical use model (N.4800)" of the Measures for the Administration of Medical Devices.

N Orthopedics

N.4800 Sample plate for clinical use

QMS/QSD;; 輸入

Dates and Status

Aug 10, 2012

Aug 10, 2017

Feb 22, 2016

Cancellation Information

Logged out

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