Taiwan FDA registration a0e6ecd92da2a24aa7c051da9b56da62
〝Teifu Spine〞I/F Lumbar Intervertebral Bone Fusion
TW: 〝帝富脊椎〞Ｉ/Ｆ腰椎椎間骨融合器
Taiwan·Risk Class 2·DEPUY SPINE, INC.·Registered Oct 27, 2000 – Oct 27, 2020CancelledRegistration details
- Analysis ID
- a0e6ecd92da2a24aa7c051da9b56da62
- Customs Code
- DHA00600954406
Company information
- Manufacturer
- DEPUY SPINE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- N000 Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2000
- Expiry Date
- Oct 27, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for 〝Teifu Spine〞I/F Lumbar Intervertebral Bone Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0e6ecd92da2a24aa7c051da9b56da62 and manufactured by DEPUY SPINE, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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