Taiwan FDA registration aa3e4e2eec6fe306b4069e7c19dfa894

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

TW: "酷達"耳鼻喉光纖光源及載具(未滅菌)

Taiwan·Risk Class 1·MD·SUNOPTIC TECHNOLOGIES, LLC·Registered Sep 11, 2013 – Sep 11, 2028Active

Registration details

Analysis ID: aa3e4e2eec6fe306b4069e7c19dfa894
License Form: Ministry of Health Medical Device Import No. 013409
Customs Code: DHA09401340902

Company information

Manufacturer: SUNOPTIC TECHNOLOGIES, LLC
Manufacturer Country: United States
Authorized Representative: TRANSMEDIC 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: Sep 11, 2013
Expiry Date: Sep 11, 2028

About this record

Access comprehensive regulatory information for "CUDA SURGICAL" 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 aa3e4e2eec6fe306b4069e7c19dfa894 and manufactured by SUNOPTIC TECHNOLOGIES, LLC. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..

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