Taiwan FDA registration 6cce27d79de3a5366d46dcb64b872cc2

"Daiichi" Ear, nose, and throat examination and treatment unit (Non-Sterile)

TW: "大壹器" 耳鼻喉檢查及治療檯 (未滅菌)

Taiwan·Risk Class 1·MD·DAIICHI MEDICAL CO., LTD.·Registered Aug 05, 2013 – Aug 05, 2023Expired

Registration details

Analysis ID: 6cce27d79de3a5366d46dcb64b872cc2
License Form: Ministry of Health Medical Device Import No. 013277
Customs Code: DHA09401327701

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 of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G5300 ENT Examination and Treatment Unit
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 05, 2013
Expiry Date: Aug 05, 2023

About this record

Access comprehensive regulatory information for "Daiichi" Ear, nose, and throat examination and treatment unit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6cce27d79de3a5366d46dcb64b872cc2 and manufactured by DAIICHI MEDICAL CO., LTD.. The authorized representative in Taiwan is GIA HO INSTRUMENTS CO., LTD..

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