Taiwan FDA registration 693675b63c11bef524d7b5c3ba2c82de
"Medtronic" Pulse Optimization Pulse Ablation Instrument and Components
TW: “美敦力” 脈優選脈衝消融儀及組件
Taiwan·Risk Class 3·Medtronic Inc.·Registered Aug 11, 2024 – Aug 11, 2029ActiveRegistration details
- Analysis ID
- 693675b63c11bef524d7b5c3ba2c82de
- Customs Code
- DHA05603727404
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.0008.
- Import Information
- import
Dates and status
- Registration Date
- Aug 11, 2024
- Expiry Date
- Aug 11, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Pulse Optimization Pulse Ablation Instrument and Components in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 693675b63c11bef524d7b5c3ba2c82de and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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