Taiwan FDA registration 913422c6f0aed90d0d9f762e0d969ab6
"Sauron" Eos blood oxygenator
TW: “索倫”伊歐斯血液氧合器
Taiwan·Risk Class 2·SORIN GROUP ITALIA S.R.L.·Registered Aug 10, 2012 – Aug 10, 2017CancelledRegistration details
- Analysis ID
- 913422c6f0aed90d0d9f762e0d969ab6
- Customs Code
- DHA00602392003
Company information
- Manufacturer
- SORIN GROUP ITALIA S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE 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.4350 Cardiopulmonary vascular bypass and oxygen apparatus
- Import Information
- import
Dates and status
- Registration Date
- Aug 10, 2012
- Expiry Date
- Aug 10, 2017
- Cancellation Date
- Nov 18, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Sauron" Eos blood oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 913422c6f0aed90d0d9f762e0d969ab6 and manufactured by SORIN GROUP ITALIA S.R.L.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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