Taiwan FDA registration 4082566e2455f0f235f4c8b257634300
"TERUMO" TERUFUSION SOLUTION ADMINISTRATION SET
TW: 輸液套
Taiwan·Risk Class 2·MD·KOFU FACTORY OF TERUMO CORPORATION·Registered Aug 02, 1999 – Nov 21, 2025ExpiredRegistration details
- Analysis ID
- 4082566e2455f0f235f4c8b257634300
- License Form
- Department of Health Medical Device Import No. 007673
- Customs Code
- DHA00600767307
Company information
- Manufacturer
- KOFU FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- 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
- Aug 02, 1999
- Expiry Date
- Nov 21, 2025
About this record
Access comprehensive regulatory information for "TERUMO" TERUFUSION SOLUTION ADMINISTRATION SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4082566e2455f0f235f4c8b257634300 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices