Taiwan FDA registration 552802318ce5e03a0361fe2c9f4ba456
"Medtronic" Anval Heart Implantable Cardiac Rectification Defibrillator System
TW: “美敦力” 安諾心植入式心臟整流去顫器系統
Taiwan·Risk Class 3·Medtronic Inc.·Registered Sep 15, 2024 – Sep 15, 2029ActiveRegistration details
- Analysis ID
- 552802318ce5e03a0361fe2c9f4ba456
- Customs Code
- DHA05603741407
Company information
- Manufacturer
- Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- import
Dates and status
- Registration Date
- Sep 15, 2024
- Expiry Date
- Sep 15, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Anval Heart Implantable Cardiac Rectification Defibrillator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 552802318ce5e03a0361fe2c9f4ba456 and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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