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"Isolux" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration d66c4eb0c7e17ca5fa14235a3d604295

Access comprehensive regulatory information for "Isolux" 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 d66c4eb0c7e17ca5fa14235a3d604295 and manufactured by ISOLUX LLC. The authorized representative in Taiwan is KINGJING INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ISOLUX LLC, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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d66c4eb0c7e17ca5fa14235a3d604295
Registration Details
Taiwan FDA Registration: d66c4eb0c7e17ca5fa14235a3d604295
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Device Details

"Isolux" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "่‰พ่Šๆ–ฝ" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d66c4eb0c7e17ca5fa14235a3d604295

Ministry of Health Medical Device Import No. 020842

DHA09402084207

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 09, 2019

Sep 09, 2024

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