Taiwan FDA registration 821009144704f146db93594b1c459776
“General” Multi-Parameter Patient Monitor
TW: “杰納瑞”多參數監視儀
Taiwan·Risk Class 2·MD·General Meditech, Inc·Registered Feb 14, 2014 – Feb 14, 2024ExpiredRegistration details
- Analysis ID
- 821009144704f146db93594b1c459776
- License Form
- Ministry of Health Medical Device Land Transport No. 000584
- Customs Code
- DHA09200058409
Company information
- Manufacturer
- General Meditech, Inc
- Manufacturer Country
- China
- Authorized Representative
- SCHMIDT SCIENTIFIC TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Feb 14, 2014
- Expiry Date
- Feb 14, 2024
About this record
Access comprehensive regulatory information for “General” Multi-Parameter Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 821009144704f146db93594b1c459776 and manufactured by General Meditech, Inc. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..
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