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"MEGA" Ear, nose and throat examination and treatment unit (Non-Sterile) - Taiwan Registration 9a8c6699961398247c8aadfbff406262

Access comprehensive regulatory information for "MEGA" Ear, nose and throat examination and treatment unit (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 9a8c6699961398247c8aadfbff406262 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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9a8c6699961398247c8aadfbff406262
Registration Details
Taiwan FDA Registration: 9a8c6699961398247c8aadfbff406262
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Device Details

"MEGA" Ear, nose and throat examination and treatment unit (Non-Sterile)
TW: "็พŽไฝณ" ่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9a8c6699961398247c8aadfbff406262

Ministry of Health Medical Device Import No. 017636

DHA09401763607

Company Information

Korea, Republic of

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".

G ENT device

G5300 ENT Examination and Treatment Unit

Imported from abroad

Dates and Status

Mar 23, 2017

Mar 23, 2022