Taiwan FDA registration a9788dfb5ad6c5b1a79b9376034b7f62
"Oshipa" cardiac hemodynamic monitor
TW: “歐希帕”心臟血液動力監視儀
Taiwan·Risk Class 2·OSYPKA MEDICAL GMBH·Registered Nov 29, 2012 – Nov 29, 2017CancelledRegistration details
- Analysis ID
- a9788dfb5ad6c5b1a79b9376034b7f62
- Customs Code
- DHA00602423700
Company information
- Manufacturer
- OSYPKA MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SUNNY HEART SCIENTIFIC 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.2770 Medical Impedance Frame Tester(Impedance Peripheral Flow Tester)
- Import Information
- import
Dates and status
- Registration Date
- Nov 29, 2012
- Expiry Date
- Nov 29, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Oshipa" cardiac hemodynamic monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9788dfb5ad6c5b1a79b9376034b7f62 and manufactured by OSYPKA MEDICAL GMBH. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC CO., LTD..
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