Taiwan FDA registration 694cb60a6ffa8432358dd592bb0507cc
"Spite" can be anterior cervical fusion device
TW: “司佰特”萃媞可前路頸椎融合器
Taiwan·Risk Class 2·SPINEART SA;; ALPES CN SAS·Registered Feb 14, 2022 – Feb 14, 2027ActiveRegistration details
- Analysis ID
- 694cb60a6ffa8432358dd592bb0507cc
- Customs Code
- DHA05603526901
Company information
- Manufacturer
- SPINEART SA;; ALPES CN SAS
- Manufacturer Country
- France;;Switzerland
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- import
Dates and status
- Registration Date
- Feb 14, 2022
- Expiry Date
- Feb 14, 2027
About this record
Access comprehensive regulatory information for "Spite" can be anterior cervical fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 694cb60a6ffa8432358dd592bb0507cc and manufactured by SPINEART SA;; ALPES CN SAS. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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