Taiwan FDA registration 40d74f8c6c308025de90d60b7214d5b9

"MUTOH" Nonpowered neurosurgical instrument (Non-Sterile)

TW: "上山" 非動力式神經外科用器械 (未滅菌)

Taiwan·Risk Class 1·MD·MUTOH AMERICA CO., LTD.·Registered Feb 15, 2017 – Feb 15, 2022Expired

Registration details

Analysis ID: 40d74f8c6c308025de90d60b7214d5b9
License Form: Ministry of Health Medical Device Import No. 017493
Customs Code: DHA09401749301

Company information

Manufacturer: MUTOH AMERICA CO., LTD.
Manufacturer Country: United States
Authorized Representative: GRAND MEDICAL INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
Product Type (Level 1): K Devices for neuroscience
Product Type (Level 2): K4535 Non-powered neurosurgical instruments
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 15, 2017
Expiry Date: Feb 15, 2022

About this record

Access comprehensive regulatory information for "MUTOH" Nonpowered neurosurgical 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 40d74f8c6c308025de90d60b7214d5b9 and manufactured by MUTOH AMERICA CO., LTD.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..

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