Taiwan FDA registration f740e3bd2f78e6ab05265b4eb7e589f3
"Ne-Yo" annular skull fixator
TW: “尼歐”環狀顱骨固定器
Taiwan·Risk Class 2·Neos Surgery S.L.·Registered Jun 18, 2013 – Jun 18, 2028ActiveRegistration details
- Analysis ID
- f740e3bd2f78e6ab05265b4eb7e589f3
- Customs Code
- DHA00602466801
Company information
- Manufacturer
- Neos Surgery S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5250 Drilled cover
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2013
- Expiry Date
- Jun 18, 2028
About this record
Access comprehensive regulatory information for "Ne-Yo" annular skull fixator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f740e3bd2f78e6ab05265b4eb7e589f3 and manufactured by Neos Surgery S.L.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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