Taiwan FDA registration ac5d217398e6e8fb32f29f080c85df2c
"Spite" Romeo Pader interspinal system
TW: “司佰特”羅密歐帕德脊突間系統
Taiwan·Risk Class 2·SPINEART SA;; ALPES CN SAS·Registered Feb 20, 2013 – Feb 20, 2028ActiveRegistration details
- Analysis ID
- ac5d217398e6e8fb32f29f080c85df2c
- Customs Code
- DHA00602474200
Company information
- Manufacturer
- SPINEART SA;; ALPES CN SAS
- Manufacturer Country
- France;;Switzerland
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
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
- Feb 20, 2013
- Expiry Date
- Feb 20, 2028
About this record
Access comprehensive regulatory information for "Spite" Romeo Pader interspinal system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac5d217398e6e8fb32f29f080c85df2c and manufactured by SPINEART SA;; ALPES CN SAS. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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