Taiwan FDA registration 410fe131f40adab9785840fe7ea28a13
"Ito" pressure supply device (unsterilized)
TW: "伊藤" 壓力供應裝置 (未滅菌)
Registration details
- Analysis ID
- 410fe131f40adab9785840fe7ea28a13
- Customs Code
- DHA04401100705
Company information
- Manufacturer
- ITO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of "pressure supply devices (O.5765)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5765 壓力供應裝置
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2011
- Expiry Date
- Nov 02, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ito" pressure supply device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 410fe131f40adab9785840fe7ea28a13 and manufactured by ITO CO., LTD.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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