Taiwan FDA registration f40c979253537c34c2ecd11f073d6a54
"Medtronic" Efis bone nail system
TW: "美敦力"艾菲思骨釘系統
Taiwan·Risk Class 2·MEDTRONIC XOMED, INC.·Registered Feb 23, 2011 – Feb 23, 2021CancelledRegistration details
- Analysis ID
- f40c979253537c34c2ecd11f073d6a54
- Customs Code
- DHA00602179809
Company information
- Manufacturer
- MEDTRONIC XOMED, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Indicated for the treatment of obstructive sleep apnea (OSA) and/or snoring. Performance changes: For details, as shown in Chinese approved copy of the imitation order (the original label approved in 101.9.11 and the approved copy of the imitation order will be recycled and invalidated).
- Product Type (Level 1)
- F Dentistry
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2011
- Expiry Date
- Feb 23, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Medtronic" Efis bone nail system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f40c979253537c34c2ecd11f073d6a54 and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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