Taiwan FDA registration fe2dd455a9edddbfce1db597d263a064
"Sauron" Cambefer evolved into an oxygenator
TW: “索倫”康倍佛進化成人氧合器
Taiwan·Risk Class 2·SORIN GROUP ITALIA S.R.L.·Registered Dec 02, 2011 – Dec 02, 2021CancelledRegistration details
- Analysis ID
- fe2dd455a9edddbfce1db597d263a064
- Customs Code
- DHA00602294807
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
- Dec 02, 2011
- Expiry Date
- Dec 02, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Sauron" Cambefer evolved into an oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe2dd455a9edddbfce1db597d263a064 and manufactured by SORIN GROUP ITALIA S.R.L.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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