Taiwan FDA registration a7416c038626078a7ae403253f5d0974
"Medtronic" Kenosin portable breath monitor
TW: “美敦力”凱諾辛攜帶式呼吸監測器
Taiwan·Risk Class 2·ORIDION MEDICAL 1987 LTD.·Registered Mar 07, 2019 – Mar 07, 2029ActiveRegistration details
- Analysis ID
- a7416c038626078a7ae403253f5d0974
- Customs Code
- DHA05603228306
Company information
- Manufacturer
- ORIDION MEDICAL 1987 LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology; E Cardiovascular Medicine Science
- Product Type (Level 2)
- D.1400 Carbon dioxide gas analysis instrument;; E.2700 Blood oxigenesis and measurement ritual
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 2019
- Expiry Date
- Mar 07, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Kenosin portable breath monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a7416c038626078a7ae403253f5d0974 and manufactured by ORIDION MEDICAL 1987 LTD.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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