Taiwan FDA registration fd3f45835b6f756c782f0c6adca48d88

"DeFara" temperature stimulator (unsterilized)

TW: "迪法拉" 溫差刺激器 (未滅菌)

Taiwan·Risk Class 1·INSTRUMENTATION DIFRA S.A.·Registered May 16, 2019 – May 16, 2029Active

Registration details

Analysis ID: fd3f45835b6f756c782f0c6adca48d88
Customs Code: DHA09402044905

Company information

Manufacturer: INSTRUMENTATION DIFRA S.A.
Manufacturer Country: Belgium
Authorized Representative: BOYANG MEDICAL TECHNOLOGY CO., LTD

Product details

Intended Use: It is limited to the first level of identification of the "Air Temperature or Water Temperature Temperature Difference Test Stimulator (G.1800)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.1800 Atmospheric or Water Temperature Differential Stimulation Device
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: May 16, 2019
Expiry Date: May 16, 2029

About this record

Access comprehensive regulatory information for "DeFara" temperature stimulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd3f45835b6f756c782f0c6adca48d88 and manufactured by INSTRUMENTATION DIFRA S.A.. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

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