Taiwan FDA registration be81fdd8374fc3f4565590167b99d5e1

"NAGASHIMA" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)

TW: "那蓋系麻" 耳鼻喉光纖光源及載具 (未滅菌)

Taiwan·Risk Class 1·MD·NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.·Registered Apr 17, 2014 – Apr 17, 2024Expired

Registration details

Analysis ID: be81fdd8374fc3f4565590167b99d5e1
License Form: Ministry of Health Medical Device Import No. 014065
Customs Code: DHA09401406501

Company information

Manufacturer: NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Japan
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: Apr 17, 2014
Expiry Date: Apr 17, 2024

About this record

Access comprehensive regulatory information for "NAGASHIMA" 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 be81fdd8374fc3f4565590167b99d5e1 and manufactured by NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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