Taiwan FDA registration da51101a1e2e0aaf3cbb6569ed8623d3
“Medtronic” DIVERGENCE Anterior Cervical Fusion System
TW: “美敦力”玳佛峻斯前側頸椎融合系統
Taiwan·Risk Class 2·MD·Medtronic Puerto Rico Operations Co., Humacao·Registered Jun 11, 2019 – Jun 11, 2024ExpiredRegistration details
- Analysis ID
- da51101a1e2e0aaf3cbb6569ed8623d3
- License Form
- Ministry of Health Medical Device Import No. 032688
- Customs Code
- DHA05603268806
Company information
- Manufacturer
- Medtronic Puerto Rico Operations Co., Humacao
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 11, 2019
- Expiry Date
- Jun 11, 2024
About this record
Access comprehensive regulatory information for “Medtronic” DIVERGENCE Anterior Cervical Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da51101a1e2e0aaf3cbb6569ed8623d3 and manufactured by Medtronic Puerto Rico Operations Co., Humacao. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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