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"MEGA" ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration 763d216d399d0a24f7f170ae81c91106

Access comprehensive regulatory information for "MEGA" 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 763d216d399d0a24f7f170ae81c91106 and manufactured by MEGA MEDICAL CO., LTD. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

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763d216d399d0a24f7f170ae81c91106
Registration Details
Taiwan FDA Registration: 763d216d399d0a24f7f170ae81c91106
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Device Details

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

Registration Details

763d216d399d0a24f7f170ae81c91106

Ministry of Health Medical Device Import No. 020361

DHA09402036104

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

Apr 24, 2019

Apr 24, 2024