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"KURZ" Prosthesis modification instrument for ossicular replacement surgery (non-sterile) - Taiwan Registration 9cdab07fd0428bd8a4ea954ff4e739a7

Access comprehensive regulatory information for "KURZ" Prosthesis modification instrument for ossicular replacement surgery (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 9cdab07fd0428bd8a4ea954ff4e739a7 and manufactured by Heinz Kurz GmbH. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..

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9cdab07fd0428bd8a4ea954ff4e739a7
Registration Details
Taiwan FDA Registration: 9cdab07fd0428bd8a4ea954ff4e739a7
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Device Details

"KURZ" Prosthesis modification instrument for ossicular replacement surgery (non-sterile)
TW: "ๅ…‹็ˆพ" ่ฝๅฐ้ชจ็ฝฎๆ›็‰ฉไฟฎๆญฃ็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9cdab07fd0428bd8a4ea954ff4e739a7

Ministry of Health Medical Device Import No. 021603

DHA09402160307

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Devices for Correction of Ossicle Replacement (G.3540)".

G ENT device

G3540 Instrument for Hearing Bone Replacement Correction

Imported from abroad

Dates and Status

Jun 01, 2020

Jun 01, 2025