Taiwan FDA registration 790e946a66a70139a73b93609f687dc3

“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)

Taiwan·Risk Class 1·MD·BOSS INSTRUMENTS, LTD.·Registered Apr 26, 2022 – Apr 26, 2027Active

Registration details

Analysis ID: 790e946a66a70139a73b93609f687dc3
License Form: Ministry of Health Medical Device Import No. 022790
Customs Code: DHA09402279001

Company information

Manufacturer: BOSS INSTRUMENTS, LTD.
Manufacturer Country: United States
Authorized Representative: GOLDENSPRING MEDI-TECH CO., LTD.

Product details

Intended Use: 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)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G3540 Instrument for Hearing Bone Replacement Correction
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 26, 2022
Expiry Date: Apr 26, 2027

About this record

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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