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"Cochlear" Ear, nose, and throat manual surgical instrument (Non-Sterile) - Taiwan Registration 8d3edba76b43e4b8594c2ca11273b254

Access comprehensive regulatory information for "Cochlear" Ear, nose, and throat manual surgical instrument (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 8d3edba76b43e4b8594c2ca11273b254 and manufactured by COCHLEAR LIMITED. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COCHLEAR LIMITED, and 1 recent registrations in the same category. 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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8d3edba76b43e4b8594c2ca11273b254
Registration Details
Taiwan FDA Registration: 8d3edba76b43e4b8594c2ca11273b254
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Device Details

"Cochlear" Ear, nose, and throat manual surgical instrument (Non-Sterile)
TW: "ๅฏ็ซ‹่€ณ" ่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8d3edba76b43e4b8594c2ca11273b254

Ministry of Health Medical Device Import No. 014704

DHA09401470409

Company Information

Australia

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad

Dates and Status

Nov 26, 2014

Nov 26, 2024

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