Taiwan FDA registration 6cdb5f7be1019b9f4ffeed90a26dce23
"Medtronic" Atlantis anterior cervical vertebrae plate system
TW: “美敦力”亞特蘭提斯前方頸椎骨板系統
Taiwan·Risk Class 2·MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·Registered Nov 26, 2009 – Nov 26, 2019CancelledRegistration details
- Analysis ID
- 6cdb5f7be1019b9f4ffeed90a26dce23
- Customs Code
- DHA00602044000
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 Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Nov 26, 2009
- Expiry Date
- Nov 26, 2019
- Cancellation Date
- Jul 10, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" Atlantis anterior cervical vertebrae plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6cdb5f7be1019b9f4ffeed90a26dce23 and manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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