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“Boss” Prosthesis modification instrument for ossicular replacement surgery (Non-Sterile) - Taiwan Registration 790e946a66a70139a73b93609f687dc3

Access comprehensive regulatory information for “Boss” 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 790e946a66a70139a73b93609f687dc3 and manufactured by BOSS INSTRUMENTS, LTD.. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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790e946a66a70139a73b93609f687dc3
Registration Details
Taiwan FDA Registration: 790e946a66a70139a73b93609f687dc3
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Device Details

“Boss” Prosthesis modification instrument for ossicular replacement surgery (Non-Sterile)
TW: “博司”聽小骨置換物修正用器械(未滅菌)
Risk Class 1
MD

Registration Details

790e946a66a70139a73b93609f687dc3

Ministry of Health Medical Device Import No. 022790

DHA09402279001

Company Information

United States

Product Details

Limited to the first level identification scope of the Classification and Grading Management Measures for Medical Devices "Devices for Correction of Small Bone Replacement (G.3540)".

G ENT Science

G3540 Instrument for Hearing Bone Replacement Correction

Imported from abroad

Dates and Status

Apr 26, 2022

Apr 26, 2027