Taiwan FDA registration 35bf60e5c9bff47541e6c8804823569f
"Qinglimei" Qinglide balloon vertebroplasty kit
TW: “擎力美”擎力得球囊椎體成形術套組
Taiwan·Risk Class 2·ZHENPENG BIOTECH CO., LTD.·Registered Aug 31, 2022 – Aug 28, 2026ActiveRegistration details
- Analysis ID
- 35bf60e5c9bff47541e6c8804823569f
Company information
- Manufacturer
- 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.0004 骨擴張成型系統
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 31, 2022
- Expiry Date
- Aug 28, 2026
About this record
Access comprehensive regulatory information for "Qinglimei" Qinglide balloon vertebroplasty kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 35bf60e5c9bff47541e6c8804823569f and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is XELITE BIOMED LTD..
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