Taiwan FDA registration 01974ac57a208f3b14ef19c4b1557b7c
Qinli Bone Cement Mixer (Sterilization)
TW: 擎力美骨水泥攪拌器 (滅菌)
Taiwan·Risk Class 1·ZHENPENG BIOTECH CO., LTD.·Registered Sep 18, 2020 – Sep 18, 2025ExpiredRegistration details
- Analysis ID
- 01974ac57a208f3b14ef19c4b1557b7c
Company information
- Manufacturer
- ZHENPENG BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- XELITE BIOMED LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Clinical Bone Cement Mixer (N.4210)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4210 臨床用骨水泥攪拌器
- Import Information
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Sep 18, 2020
- Expiry Date
- Sep 18, 2025
About this record
Access comprehensive regulatory information for Qinli Bone Cement Mixer (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 01974ac57a208f3b14ef19c4b1557b7c and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is XELITE BIOMED LTD..
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