Taiwan FDA registration cc46a028d5abe7f80ad6073a7e2f9733
"Spite" cervical intervertebral implants
TW: “司佰特”頸椎椎間植入物
Taiwan·Risk Class 2·SPINEART SA;; ALPES CN SAS·Registered Sep 15, 2010 – Sep 15, 2025ExpiredRegistration details
- Analysis ID
- cc46a028d5abe7f80ad6073a7e2f9733
- Customs Code
- DHA00602146001
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
- Sep 15, 2010
- Expiry Date
- Sep 15, 2025
About this record
Access comprehensive regulatory information for "Spite" cervical intervertebral implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc46a028d5abe7f80ad6073a7e2f9733 and manufactured by SPINEART SA;; ALPES CN SAS. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices