Taiwan FDA registration 8b06ab48125435c47c9ab0e095c05ad1
"Ashyou" Digo catheter device
TW: “艾希優”迪高導管裝置
Taiwan·Risk Class 2·ICU MEDICAL, INC.·Registered Feb 06, 2020 – Feb 06, 2025ExpiredRegistration details
- Analysis ID
- 8b06ab48125435c47c9ab0e095c05ad1
- Customs Code
- DHA05603323500
Company information
- Manufacturer
- ICU MEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ICU MEDICAL B.V., TAIWAN BRANCH (NETHERLANDS)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment;; H Gastroenterology and Urology
- Product Type (Level 2)
- J.5440 血管內輸液套;; H.5540 血液通路裝置及其附件
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2020
- Expiry Date
- Feb 06, 2025
About this record
Access comprehensive regulatory information for "Ashyou" Digo catheter device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b06ab48125435c47c9ab0e095c05ad1 and manufactured by ICU MEDICAL, INC.. The authorized representative in Taiwan is ICU MEDICAL B.V., TAIWAN BRANCH (NETHERLANDS).
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