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"Cochlear" Ear manual surgical instrument (Non-Sterile) - Taiwan Registration 985350f4573b840e5195761d4b90e73f

Access comprehensive regulatory information for "Cochlear" Ear 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 985350f4573b840e5195761d4b90e73f and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is CLINICO INC..

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985350f4573b840e5195761d4b90e73f
Registration Details
Taiwan FDA Registration: 985350f4573b840e5195761d4b90e73f
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Device Details

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

Registration Details

985350f4573b840e5195761d4b90e73f

Ministry of Health Medical Device Import No. 013744

DHA09401374403

Company Information

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

Jan 03, 2014

Jan 03, 2024