Taiwan FDA registration 797f7c4c1484cd8e34829fc519995813
“Terumo” Destination Guiding Sheath
TW: “泰爾茂”諦思迪迅導引套
Taiwan·Risk Class 2·MD·TERUMO MEDICAL CORPORATION·Registered Aug 07, 2013 – Aug 07, 2028ActiveRegistration details
- Analysis ID
- 797f7c4c1484cd8e34829fc519995813
- License Form
- Ministry of Health Medical Device Import No. 025221
- Customs Code
- DHA05602522106
Company information
- Manufacturer
- TERUMO MEDICAL CORPORATION
- 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)
- E1340 Catheter Guide
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2013
- Expiry Date
- Aug 07, 2028
About this record
Access comprehensive regulatory information for “Terumo” Destination Guiding Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 797f7c4c1484cd8e34829fc519995813 and manufactured by TERUMO MEDICAL 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