Taiwan FDA registration 8e17048f26290e286660e0922deb3fd8

"Smith" Heat and Moisture Condenser (Artificial Nose) (Sterilization)

TW: “史密斯” 熱及濕氣凝結器 (人工鼻)(滅菌)
Taiwan flagTaiwan·Risk Class 1·Smiths Medical Czech Republic a.s.·Registered Jul 19, 2017 – Jul 19, 2022Cancelled
Registration details
Analysis ID
8e17048f26290e286660e0922deb3fd8
Customs Code
DHA09401808208
Company information
Manufacturer Country
Czechia
Authorized Representative
RADIANT MEDICAL COMPANY
Product details
Intended Use
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5375 Heat and humidity condenser (artificial nose)
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jul 19, 2017
Expiry Date
Jul 19, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Smith" Heat 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 8e17048f26290e286660e0922deb3fd8 and manufactured by Smiths Medical Czech Republic a.s.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITHS HEALTHCARE MANUFACTURING SA DE CV, and 1 recent registrations in the same category. 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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