Taiwan FDA registration b8801ad765f1677f1d9dfd7bd437e2a5
"Genari" multi-parameter monitor
TW: “杰納瑞”多參數監視儀
Registration details
- Analysis ID
- b8801ad765f1677f1d9dfd7bd437e2a5
- Customs Code
- DHA09200058409
Company information
- Manufacturer
- General Meditech, Inc
- Manufacturer Country
- China
- Authorized Representative
- Schming Scientific Company Limited
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.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 14, 2014
- Expiry Date
- Feb 14, 2029
About this record
Access comprehensive regulatory information for "Genari" multi-parameter monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b8801ad765f1677f1d9dfd7bd437e2a5 and manufactured by General Meditech, Inc. The authorized representative in Taiwan is Schming Scientific Company Limited.
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