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"Meijia" ENT Examination and Treatment Device (Unsterilized) - Taiwan Registration 38b1b228c5a0657c2f6cc2d667172985

Access comprehensive regulatory information for "Meijia" ENT Examination and Treatment Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38b1b228c5a0657c2f6cc2d667172985 and manufactured by MEGA MEDICAL CO., LTD. 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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38b1b228c5a0657c2f6cc2d667172985
Registration Details
Taiwan FDA Registration: 38b1b228c5a0657c2f6cc2d667172985
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Device Details

"Meijia" ENT Examination and Treatment Device (Unsterilized)
TW: ใ€็พŽไฝณใ€ž่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

38b1b228c5a0657c2f6cc2d667172985

DHA04400322608

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices (ENT Examination and Treatment Table [G.5300]).

G ENT Science

G.5300 ENT examination and treatment table

import

Dates and Status

Mar 28, 2006

Mar 28, 2021

Aug 28, 2023

Cancellation Information

Logged out

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