Taiwan FDA registration c899c4e27dc9c5b87b868cc568633eb9

"Big One Device" ENT Examination & Treatment Table (Non-sterilized)

TW: "大壹器" 耳鼻喉檢查及治療檯(未滅菌)

Taiwan·Risk Class 1·DAIICHI MEDICAL CO., LTD.·Registered Aug 23, 2023 – Aug 23, 2028Active

Registration details

Analysis ID: c899c4e27dc9c5b87b868cc568633eb9
Customs Code: DHA09402321702

Company information

Manufacturer: DAIICHI MEDICAL CO., LTD.
Manufacturer Country: Japan
Authorized Representative: GIA HO INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "ENT Examination and Treatment Unit (G.5300)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5300 ENT examination and treatment table
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Aug 23, 2023
Expiry Date: Aug 23, 2028

About this record

Access comprehensive regulatory information for "Big One Device" ENT Examination & Treatment Table (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c899c4e27dc9c5b87b868cc568633eb9 and manufactured by DAIICHI MEDICAL CO., LTD.. The authorized representative in Taiwan is GIA HO INSTRUMENTS CO., LTD..

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