Taiwan FDA registration dd857d4bffe9cc13a74dab9b6ebd4f3e
“Terumo” Capiox FX advance Oxygenator
TW: “泰爾茂” 菲斯新一代氧合器
Taiwan·Risk Class 2·MD·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Registered Apr 07, 2021 – Apr 07, 2026ExpiredRegistration details
- Analysis ID
- dd857d4bffe9cc13a74dab9b6ebd4f3e
- License Form
- Ministry of Health Medical Device Import No. 034488
- Customs Code
- DHA05603448808
Company information
- Manufacturer
- TERUMO CARDIOVASCULAR SYSTEMS CORP.
- 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
- Apr 07, 2021
- Expiry Date
- Apr 07, 2026
About this record
Access comprehensive regulatory information for “Terumo” Capiox FX advance Oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd857d4bffe9cc13a74dab9b6ebd4f3e and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORP.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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