Taiwan FDA registration 38c6dec234fa51be5f6ca6a452a57218
"Femas" non-invasive blood pressure monitoring system
TW: "菲瑪斯" 非侵入式血壓監檢測系統
Registration details
- Analysis ID
- 38c6dec234fa51be5f6ca6a452a57218
- Customs Code
- DHA00601248003
Company information
- Manufacturer
- FMS, FINAPRES MEDICL SYSTEMS B. V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- JINGS INSTRUMENT 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
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2005
- Expiry Date
- Oct 04, 2010
- Cancellation Date
- Oct 31, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Femas" non-invasive blood pressure monitoring system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 38c6dec234fa51be5f6ca6a452a57218 and manufactured by FMS, FINAPRES MEDICL SYSTEMS B. V.. The authorized representative in Taiwan is JINGS INSTRUMENT 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