Taiwan FDA registration bd637cd465409626fe5bd9417a7be32f
XeliteMed BondFix Bone Cement (Sterile)
TW: 擎力美椎體骨水泥(滅菌)
Taiwan·Risk Class 2·MD·ZHENPENG BIOTECH CO., LTD.·Registered Jul 10, 2018 – Jul 10, 2028ActiveRegistration details
- Analysis ID
- bd637cd465409626fe5bd9417a7be32f
- License Form
- Ministry of Health Medical Device Manufacturing No. 006161
Company information
- Manufacturer
- ZHENPENG BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- XELITE BIOMED LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3027 PMMA bone cement
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jul 10, 2018
- Expiry Date
- Jul 10, 2028
About this record
Access comprehensive regulatory information for XeliteMed BondFix Bone Cement (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd637cd465409626fe5bd9417a7be32f and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is XELITE BIOMED LTD..
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