Taiwan FDA registration fe492ff8d68fc2f6bb92e08f8a317e33

"Gulev" ENT fiber optic light source and vehicle (unsterilized)

TW: “古樂夫”耳鼻喉光纖光源及載具(未滅菌)

Taiwan·Risk Class 1·GULF MEDICAL FIBEROPTICS, INC.·Registered Dec 07, 2012 – Dec 07, 2017Cancelled

Registration details

Analysis ID: fe492ff8d68fc2f6bb92e08f8a317e33
Customs Code: DHA04401245501

Company information

Manufacturer: GULF MEDICAL FIBEROPTICS, INC.
Manufacturer Country: United States
Authorized Representative: Chenyu Technology 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 Science
Product Type (Level 2): G.4350 Ear, nose and throat optical fiber light sources and carriers
Import Information: import

Dates and status

Registration Date: Dec 07, 2012
Expiry Date: Dec 07, 2017
Cancellation Date: Nov 20, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Gulev" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe492ff8d68fc2f6bb92e08f8a317e33 and manufactured by GULF MEDICAL FIBEROPTICS, INC.. The authorized representative in Taiwan is Chenyu Technology Co., Ltd.

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