Taiwan FDA registration 4869f33d95985b320f3cce1dd42d944b
"Medtronic" Maximon implantable defibrous fibrillation system
TW: "美敦力" 麥思蒙植入式去纖維顫動系統
Taiwan·MEDTRONIC EUROPE SARL·Registered Mar 22, 2005 – Mar 22, 2010CancelledRegistration details
- Analysis ID
- 4869f33d95985b320f3cce1dd42d944b
- Customs Code
- DHA00601111402
Company information
- Manufacturer
- MEDTRONIC EUROPE SARL
- Manufacturer Country
- Switzerland
- Authorized Representative
- Medtronic Medical Products Inc.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Mar 22, 2005
- Expiry Date
- Mar 22, 2010
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" Maximon implantable defibrous fibrillation system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 4869f33d95985b320f3cce1dd42d944b and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is Medtronic Medical Products Inc..
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