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"Sandek" ENT Examination and Treatment Unit (Unsterilized) - Taiwan Registration 2f609274f86b78446683e6c9bbee08f6

Access comprehensive regulatory information for "Sandek" ENT Examination and Treatment Unit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f609274f86b78446683e6c9bbee08f6 and manufactured by SOMETECH INC.. 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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2f609274f86b78446683e6c9bbee08f6
Registration Details
Taiwan FDA Registration: 2f609274f86b78446683e6c9bbee08f6
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Device Details

"Sandek" ENT Examination and Treatment Unit (Unsterilized)
TW: โ€œๆก‘ๅพ—ๅ…‹โ€่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2f609274f86b78446683e6c9bbee08f6

DHA04400492309

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 Science

G.5300 ENT examination and treatment table

import

Dates and Status

Jul 18, 2006

Jul 18, 2011

Nov 27, 2012

Cancellation Information

Logged out

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