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"Cochlear" Ear, nose, and throat manual surgical instrument (Non-Sterile) - Taiwan Registration bcf88122af7746f55ed4a90685fe4931

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 bcf88122af7746f55ed4a90685fe4931 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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bcf88122af7746f55ed4a90685fe4931
Registration Details
Taiwan FDA Registration: bcf88122af7746f55ed4a90685fe4931
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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

bcf88122af7746f55ed4a90685fe4931

Ministry of Health Medical Device Import No. 014705

DHA09401470501

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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