Taiwan FDA registration 55149ee96c3b8358f6399fc98277083b
"Spite" lumbar intervertebral disc implants
TW: “司佰特”腰椎椎間盤植入物
Taiwan·Risk Class 2·SPINEART SA·Registered Sep 23, 2010 – Sep 23, 2020CancelledRegistration details
- Analysis ID
- 55149ee96c3b8358f6399fc98277083b
- Customs Code
- DHA00602148300
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
- Sep 23, 2010
- Expiry Date
- Sep 23, 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 intervertebral disc implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55149ee96c3b8358f6399fc98277083b and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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