Taiwan FDA registration f842ca3d62d8c9b2d2b0b617c56f0ccb
"Smith" blood transfusion compression bag (unsterilized)
TW: “史密斯” 輸血加壓袋 (未滅菌)
Taiwan·Risk Class 1·SMITHS MEDICAL ASD, INC.·Registered Dec 03, 2015 – Dec 03, 2025ExpiredRegistration details
- Analysis ID
- f842ca3d62d8c9b2d2b0b617c56f0ccb
- Customs Code
- DHA09401592708
Company information
- Manufacturer
- SMITHS MEDICAL ASD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RADIANT MEDICAL COMPANY
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "Pressure apparatus for intravenous infusion bags (J.5420)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5420 靜脈輸液袋用壓力器
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 03, 2015
- Expiry Date
- Dec 03, 2025
About this record
Access comprehensive regulatory information for "Smith" blood transfusion compression bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f842ca3d62d8c9b2d2b0b617c56f0ccb and manufactured by SMITHS MEDICAL ASD, INC.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.
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