Taiwan FDA registration ea91341abeca7fcdd1097b468088263c
“Nipro” Guideplus 2 Guide extension catheter
TW: “尼普洛”蓋普拉斯第二代導引延長導管
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Oct 27, 2021 – Oct 27, 2026ActiveRegistration details
- Analysis ID
- ea91341abeca7fcdd1097b468088263c
- License Form
- Ministry of Health Medical Device Import No. 035010
- Customs Code
- DHA05603501002
Company information
- Manufacturer
- Nipro Corporation Odate Factory
- Manufacturer Country
- Japan
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 27, 2021
- Expiry Date
- Oct 27, 2026
About this record
Access comprehensive regulatory information for “Nipro” Guideplus 2 Guide extension catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea91341abeca7fcdd1097b468088263c and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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