Taiwan FDA registration 0b75ed6381dc472e9667077dc3036e15
"TERUMO" CDI HEMATOCRIT/SATURATIN CUVETTE
TW: 血氧感知器
Taiwan·Risk Class 2·MD·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Registered Sep 10, 1999 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- 0b75ed6381dc472e9667077dc3036e15
- License Form
- Department of Health Medical Device Import No. 009298
- Customs Code
- DHA00600929804
Company information
- Manufacturer
- TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- 1399 Other blood transfusion, infusion equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 1999
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "TERUMO" CDI HEMATOCRIT/SATURATIN CUVETTE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b75ed6381dc472e9667077dc3036e15 and manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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