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"Smith" Prodöderm Thermal and Moisture Condenser (Artificial Nose) (Sterilization) - Taiwan Registration ef143cc493b7f76986082b123e57b258

Access comprehensive regulatory information for "Smith" Prodöderm Thermal and Moisture Condenser (Artificial Nose) (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef143cc493b7f76986082b123e57b258 and manufactured by SMITHS MEDICAL INTERNATIONAL LTD.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

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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ef143cc493b7f76986082b123e57b258
Registration Details
Taiwan FDA Registration: ef143cc493b7f76986082b123e57b258
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Device Details

"Smith" Prodöderm Thermal and Moisture Condenser (Artificial Nose) (Sterilization)
TW: “史密斯”保德士熱及濕氣凝結器 (人工鼻)(滅菌)
Risk Class 1
Cancelled

Registration Details

ef143cc493b7f76986082b123e57b258

DHA09401344009

Company Information

United Kingdom

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".

D Anesthesiology

D.5375 Heat and humidity condenser (artificial nose)

QMS/QSD;; 輸入

Dates and Status

Sep 18, 2013

Sep 18, 2018

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者