Taiwan FDA registration c76984854a9b499752f65cc53f102d5d
“Terumo” Capiox RX Oxygenator
TW: “泰爾茂” 氧合器
Taiwan·Risk Class 2·MD·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Registered Feb 01, 2021 – Feb 01, 2026ExpiredRegistration details
- Analysis ID
- c76984854a9b499752f65cc53f102d5d
- License Form
- Ministry of Health Medical Device Import No. 034318
- Customs Code
- DHA05603431809
Company information
- Manufacturer
- TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4350 Cardiopulmonary vascular bypass and oxygen apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2021
- Expiry Date
- Feb 01, 2026
About this record
Access comprehensive regulatory information for “Terumo” Capiox RX Oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c76984854a9b499752f65cc53f102d5d and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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