Taiwan FDA registration 63c7876f192eec6f625c37d096790717
“Medtronic” AVIVO Mobile Patient Management (MPM) System
TW: “美敦力”艾維芙行動式個人監護管理系統
Taiwan·Risk Class 2·MD·Medtronic Monitoring, Inc.·Registered Jul 19, 2017 – Jul 19, 2022CancelledRegistration details
- Analysis ID
- 63c7876f192eec6f625c37d096790717
- License Form
- Ministry of Health Medical Device Import No. 029977
- Customs Code
- DHA05602997703
Company information
- Manufacturer
- Medtronic Monitoring, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1025 Arrhythmia detector and alert
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 19, 2017
- Expiry Date
- Jul 19, 2022
- Cancellation Date
- Mar 14, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Medtronic” AVIVO Mobile Patient Management (MPM) System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 63c7876f192eec6f625c37d096790717 and manufactured by Medtronic Monitoring, Inc.. 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