Taiwan FDA registration a449592dcd34fe9de3f6431e4b5af686

"MEDIANA" Ear, Nose, and Throat Fiberoptic Light Source and Carrier (Non-Sterile)

TW: "美帝那" 耳鼻喉光纖光源及載具 (未滅菌)

Taiwan·Risk Class 1·MD·Mediana Co., Ltd.·Registered Jun 12, 2017 – Jun 12, 2022Expired

Registration details

Analysis ID: a449592dcd34fe9de3f6431e4b5af686
License Form: Ministry of Health Medical Device Import No. 017945
Customs Code: DHA09401794507

Company information

Manufacturer: Mediana Co., Ltd.
Manufacturer Country: Korea, Republic of
Authorized Representative: WHOLE WELL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4350 ENT fiber optic light source and vehicle
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 12, 2017
Expiry Date: Jun 12, 2022

About this record

Access comprehensive regulatory information for "MEDIANA" Ear, Nose, and Throat Fiberoptic Light Source and Carrier (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 a449592dcd34fe9de3f6431e4b5af686 and manufactured by Mediana Co., Ltd.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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