Taiwan FDA registration 3f60ef069759702563afea6915186f5a
"TERUMO" CAPIOX ARTERIAL FILTER
TW: 動脈過濾器
Taiwan·Risk Class 2·MD·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Jul 22, 1997 – Feb 09, 2024ExpiredRegistration details
- Analysis ID
- 3f60ef069759702563afea6915186f5a
- License Form
- Department of Health Medical Device Import No. 008337
- Customs Code
- DHA00600833709
Company information
- Manufacturer
- ASHITAKA FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- ．
- Product Type (Level 1)
- 1310 Transfusion Filter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 22, 1997
- Expiry Date
- Feb 09, 2024
About this record
Access comprehensive regulatory information for "TERUMO" CAPIOX ARTERIAL FILTER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f60ef069759702563afea6915186f5a and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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