Taiwan FDA registration 0f8e7f0d65fc12265ddcf976f9f2f050
"Medtronic" One Press Serter
TW: "美敦力" 一按式輔助器
Taiwan·Risk Class 2·MD·MEDTRONIC MINIMED·Registered Jan 17, 2019 – Jan 17, 2024ExpiredRegistration details
- Analysis ID
- 0f8e7f0d65fc12265ddcf976f9f2f050
- License Form
- Ministry of Health Medical Device Import No. 032127
- Customs Code
- DHA05603212705
Company information
- Manufacturer
- MEDTRONIC MINIMED
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- This product is used to assist in the insertion of the "Medtronic" Inlet blood glucose sensor (Weibe Medical Device No. 027206). This product is suitable for a single patient and is not suitable for multiple patients.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1345 Glucose Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 17, 2019
- Expiry Date
- Jan 17, 2024
About this record
Access comprehensive regulatory information for "Medtronic" One Press Serter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f8e7f0d65fc12265ddcf976f9f2f050 and manufactured by MEDTRONIC MINIMED. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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