Taiwan FDA registration 8bcc026bc899d0f55395ed03f3219fd3
"Misio" non-powered neurosurgical instruments (unsterilized)
TW: "米斯奧" 非動力式神經外科用器械(未滅菌)
Registration details
- Analysis ID
- 8bcc026bc899d0f55395ed03f3219fd3
- Customs Code
- DHA04400996906
Company information
- Manufacturer
- MIZUHO AMERICA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Jiatai Medical Equipment 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 Neuroscience
- Product Type (Level 2)
- K.4535 非動力式神經外科用器械
- Import Information
- import
Dates and status
- Registration Date
- Mar 02, 2011
- Expiry Date
- Mar 02, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Misio" non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8bcc026bc899d0f55395ed03f3219fd3 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is Jiatai Medical Equipment 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