Taiwan FDA registration 621cfc3150e5ad0db3266a213ada509b
“SPINEART” SCARLET AC-T Implants
TW: “司佰特”史嘉雷頸椎植入物
Taiwan·Risk Class 2·MD·SPINEART SA·Registered Jul 24, 2014 – Jul 24, 2024ExpiredRegistration details
- Analysis ID
- 621cfc3150e5ad0db3266a213ada509b
- License Form
- Ministry of Health Medical Device Import No. 026352
- Customs Code
- DHA05602635200
Company information
- Manufacturer
- SPINEART SA
- Manufacturer Country
- 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 Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 24, 2014
- Expiry Date
- Jul 24, 2024
About this record
Access comprehensive regulatory information for “SPINEART” SCARLET AC-T Implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 621cfc3150e5ad0db3266a213ada509b and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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