Taiwan FDA registration 46f2b6f2292ab38c321da650bc2161ff
"Nissei" non-invasive electronic blood pressure monitor
TW: “日精”非侵入性電子血壓計
Taiwan·Risk Class 2·NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY·Registered Jul 28, 2011 – Jul 28, 2021CancelledRegistration details
- Analysis ID
- 46f2b6f2292ab38c321da650bc2161ff
- Customs Code
- DHA00602265301
Company information
- Manufacturer
- NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- YIH JIANG ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1130.
- Import Information
- import
Dates and status
- Registration Date
- Jul 28, 2011
- Expiry Date
- Jul 28, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Nissei" non-invasive electronic blood pressure monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46f2b6f2292ab38c321da650bc2161ff and manufactured by NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY. The authorized representative in Taiwan is YIH JIANG 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.
Free DatabasePowered by Pure Global AI89,000+ Devices