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"CUDA SURGICAL" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration aa3e4e2eec6fe306b4069e7c19dfa894

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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aa3e4e2eec6fe306b4069e7c19dfa894
Registration Details
Taiwan FDA Registration: aa3e4e2eec6fe306b4069e7c19dfa894
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Device Details

"CUDA SURGICAL" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "้…ท้”"่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

aa3e4e2eec6fe306b4069e7c19dfa894

Ministry of Health Medical Device Import No. 013409

DHA09401340902

Company Information

United States

Product Details

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)".

G ENT device

G4350 ENT fiber optic light source and vehicle

Imported from abroad

Dates and Status

Sep 11, 2013

Sep 11, 2028