Taiwan FDA registration 3871ba017d373636343bb09543a34636
"Qingli Meshubosi" vertebral bone cement
TW: “擎力美舒柏司”椎體用骨水泥
Taiwan·Risk Class 2·Kinrui Bio Limited;; Zhenpeng Biotech Co., Ltd·Registered Apr 19, 2024 – Apr 19, 2029ActiveRegistration details
- Analysis ID
- 3871ba017d373636343bb09543a34636
Company information
- Manufacturer
- Kinrui Bio Limited;; Zhenpeng Biotech Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- XELITE BIOMED LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3027 PMMA骨水泥
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Apr 19, 2024
- Expiry Date
- Apr 19, 2029
About this record
Access comprehensive regulatory information for "Qingli Meshubosi" vertebral 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 3871ba017d373636343bb09543a34636 and manufactured by Kinrui Bio Limited;; Zhenpeng Biotech Co., Ltd. The authorized representative in Taiwan is XELITE BIOMED LTD..
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