Taiwan FDA registration 299c5e61dc9a161db93d51f9a7ed2e48
"Spite" lumbar fusion device
TW: “司佰特”腰椎融合器
Taiwan·Risk Class 2·SPINEART SA·Registered Nov 04, 2010 – Nov 04, 2020CancelledRegistration details
- Analysis ID
- 299c5e61dc9a161db93d51f9a7ed2e48
- Customs Code
- DHA00602163507
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 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
- Nov 04, 2010
- Expiry Date
- Nov 04, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Spite" lumbar 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 299c5e61dc9a161db93d51f9a7ed2e48 and manufactured by SPINEART SA. 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