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"M.I.ONE" EAR, NOSE, AND THROAT FIBEROPTIC LIGHT SOURCE AND CARRIER (Non-Sterile) - Taiwan Registration bd5406cd99c4f614aae522e60001c7bf

Access comprehensive regulatory information for "M.I.ONE" 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 bd5406cd99c4f614aae522e60001c7bf and manufactured by M.I.ONE CO., LTD. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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bd5406cd99c4f614aae522e60001c7bf
Registration Details
Taiwan FDA Registration: bd5406cd99c4f614aae522e60001c7bf
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Device Details

"M.I.ONE" EAR, NOSE, AND THROAT FIBEROPTIC LIGHT SOURCE AND CARRIER (Non-Sterile)
TW: "ๆฉ่‰พ่ฌ"่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bd5406cd99c4f614aae522e60001c7bf

Ministry of Health Medical Device Import No. 014851

DHA09401485109

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

Jan 14, 2015

Jan 14, 2025