Taiwan FDA registration 739ce232c769424d49dc1e65ab6e4633
"Pushen" Paralos bone cement
TW: “紐伸”帕拉樂斯骨水泥
Taiwan·Risk Class 2·NEUROTHERM INC.·Registered Aug 24, 2009 – Aug 24, 2019CancelledRegistration details
- Analysis ID
- 739ce232c769424d49dc1e65ab6e4633
- Customs Code
- DHA00602013508
Company information
- Manufacturer
- NEUROTHERM INC.
- Manufacturer Country
- United States
- Authorized Representative
- JUBILANT SUNRISE SCIENTIFIC CO., LTD.
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.3027 PMMA骨水泥
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Pushen" Paralos bone cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 739ce232c769424d49dc1e65ab6e4633 and manufactured by NEUROTHERM INC.. The authorized representative in Taiwan is JUBILANT SUNRISE SCIENTIFIC CO., LTD..
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