Taiwan FDA registration 0ad0b59552dc0c27dc57e51179997884

"MURANAKA" Nonpowered neurosurgical instrument (Non-Sterile)

TW: "瑪拉那卡"非動力式神經外科用器械 (未滅菌)

Taiwan·Risk Class 1·MD·MURANAKA MEDICAL INSTRUMENTS CO., LTD.·Registered Jun 17, 2015 – Jun 17, 2025Expired

Registration details

Analysis ID: 0ad0b59552dc0c27dc57e51179997884
License Form: Ministry of Health Medical Device Import No. 015355
Customs Code: DHA09401535502

Company information

Manufacturer: MURANAKA MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Japan
Authorized Representative: BARRY TEC ENTERPRISE 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: Jun 17, 2015
Expiry Date: Jun 17, 2025

About this record

Access comprehensive regulatory information for "MURANAKA" 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 0ad0b59552dc0c27dc57e51179997884 and manufactured by MURANAKA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.