Taiwan FDA registration da8891b6507415df85f5344e06bb07a8
"Medtronic" Sinco cardiac resynchronization rhythm
TW: “美敦力”信可心臟再同步節律器
Taiwan·Risk Class 3·MEDTRONIC EUROPE SARL·Registered Nov 23, 2010 – Nov 23, 2025CancelledRegistration details
- Analysis ID
- da8891b6507415df85f5344e06bb07a8
- Customs Code
- DHA00602172600
Company information
- Manufacturer
- MEDTRONIC EUROPE SARL
- Manufacturer Country
- Switzerland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Nov 23, 2010
- Expiry Date
- Nov 23, 2025
- Cancellation Date
- Oct 21, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" Sinco cardiac resynchronization rhythm in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number da8891b6507415df85f5344e06bb07a8 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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