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"Meijia" ENT Fiber Optic Light Source and Vehicle (Unsterilized) - Taiwan Registration c0a9a2af4c5393b22e5cc7aa67ce8ea8

Access comprehensive regulatory information for "Meijia" ENT Fiber Optic Light Source and Vehicle (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0a9a2af4c5393b22e5cc7aa67ce8ea8 and manufactured by MEGA MEDICAL. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

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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c0a9a2af4c5393b22e5cc7aa67ce8ea8
Registration Details
Taiwan FDA Registration: c0a9a2af4c5393b22e5cc7aa67ce8ea8
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Device Details

"Meijia" ENT Fiber Optic Light Source and Vehicle (Unsterilized)
TW: "็พŽไฝณ" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c0a9a2af4c5393b22e5cc7aa67ce8ea8

DHA04401264707

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 Science

G.4350 Ear, nose and throat optical fiber light sources and carriers

import

Dates and Status

Jan 29, 2013

Jan 29, 2018

Nov 26, 2019

Cancellation Information

Logged out

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