Taiwan FDA registration d2756938717a8369cb4177d40182a490
"Mizuho America" Nonpowered neurosurgical instrument (Non-Sterile)
TW: "美津后" 非動力式神經外科用器械 (未滅菌)
Taiwan·Risk Class 1·MD·MIZUHO AMERICA, INC.·Registered Dec 07, 2020 – Dec 07, 2025ExpiredRegistration details
- Analysis ID
- d2756938717a8369cb4177d40182a490
- License Form
- Ministry of Health Medical Device Import No. 022160
- Customs Code
- DHA09402216004
Company information
- Manufacturer
- MIZUHO AMERICA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RUI-HUNG INSTRUMENTS 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
- Dec 07, 2020
- Expiry Date
- Dec 07, 2025
About this record
Access comprehensive regulatory information for "Mizuho America" 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 d2756938717a8369cb4177d40182a490 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is RUI-HUNG INSTRUMENTS CO., LTD..
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