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"MEDIANA" Ear, Nose, and Throat Fiberoptic Light Source and Carrier (Non-Sterile) - Taiwan Registration a449592dcd34fe9de3f6431e4b5af686

Access comprehensive regulatory information for "MEDIANA" 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 a449592dcd34fe9de3f6431e4b5af686 and manufactured by Mediana Co., Ltd.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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a449592dcd34fe9de3f6431e4b5af686
Registration Details
Taiwan FDA Registration: a449592dcd34fe9de3f6431e4b5af686
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Device Details

"MEDIANA" Ear, Nose, and Throat Fiberoptic Light Source and Carrier (Non-Sterile)
TW: "็พŽๅธ้‚ฃ" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a449592dcd34fe9de3f6431e4b5af686

Ministry of Health Medical Device Import No. 017945

DHA09401794507

Company Information

Korea, Republic of

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

Jun 12, 2017

Jun 12, 2022