Taiwan FDA registration 0ddd01c4fbab7b9cd9d30705ae5d4460
"Mizuho" Nonpowered Neurosurgical Instruments (Non-Sterile)
TW: "瑞穗" 非動力式神經外科用器械 (未滅菌)
Taiwan·Risk Class 1·MD·MIZUHO AMERICA, INC.·Registered May 31, 2019 – May 31, 2024ExpiredRegistration details
- Analysis ID
- 0ddd01c4fbab7b9cd9d30705ae5d4460
- License Form
- Ministry of Health Medical Device Import No. 020509
- Customs Code
- DHA09402050900
Company information
- Manufacturer
- MIZUHO AMERICA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FU TAI TRADING 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
- May 31, 2019
- Expiry Date
- May 31, 2024
About this record
Access comprehensive regulatory information for "Mizuho" Nonpowered Neurosurgical Instruments (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 0ddd01c4fbab7b9cd9d30705ae5d4460 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is FU TAI TRADING 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.
Free DatabasePowered by Pure Global AI89,000+ Devices