Taiwan FDA registration aa4ad4a4c9a3932131407e818b958dc3
"Termao" Spistrong Aputia Exchange Set
TW: “泰爾茂”思倍壯亞普緹亞交換套組
Taiwan·Risk Class 2·Terumo BCT, Ltd.·Registered Jan 18, 2012 – Jan 18, 2017CancelledRegistration details
- Analysis ID
- aa4ad4a4c9a3932131407e818b958dc3
- Customs Code
- DHA00602320301
Company information
- Manufacturer
- Terumo BCT, Ltd.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Taipei Branch of Nissho Termo Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9100 Containers for the collection and disposal of blood and blood components
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Jan 18, 2017
- Cancellation Date
- Aug 19, 2016
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Termao" Spistrong Aputia Exchange Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa4ad4a4c9a3932131407e818b958dc3 and manufactured by Terumo BCT, Ltd.. The authorized representative in Taiwan is Taipei Branch of Nissho Termo 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