Taiwan FDA registration b427c4cde43309918a6063acd424e401

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

TW: "高爾夫" 耳鼻喉光纖光源及載具(未滅菌)

Taiwan·Risk Class 1·MD·GULF FIBEROPTICS, INC.·Registered Dec 09, 2016 – Dec 09, 2021Expired

Registration details

Analysis ID: b427c4cde43309918a6063acd424e401
License Form: Ministry of Health Medical Device Import No. 017260
Customs Code: DHA09401726001

Company information

Manufacturer: GULF FIBEROPTICS, INC.
Manufacturer Country: United States
Authorized Representative: EVOLUTION WORLDWIDE 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: Dec 09, 2016
Expiry Date: Dec 09, 2021

About this record

Access comprehensive regulatory information for "Gulf" 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 b427c4cde43309918a6063acd424e401 and manufactured by GULF FIBEROPTICS, INC.. The authorized representative in Taiwan is EVOLUTION WORLDWIDE CO., LTD..

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