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Qinli Bone Cement Mixer (Sterilization) - Taiwan Registration 01974ac57a208f3b14ef19c4b1557b7c

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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01974ac57a208f3b14ef19c4b1557b7c
Registration Details
Taiwan FDA Registration: 01974ac57a208f3b14ef19c4b1557b7c
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Device Details

Qinli Bone Cement Mixer (Sterilization)
TW: ๆ“ŽๅŠ›็พŽ้ชจๆฐดๆณฅๆ”ชๆ‹Œๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

01974ac57a208f3b14ef19c4b1557b7c

Company Information

Taiwan, Province of China

Product Details

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.

N Orthopedics

N.4210 ่‡จๅบŠ็”จ้ชจๆฐดๆณฅๆ”ชๆ‹Œๅ™จ

ๅœ‹็”ข;; ๅง”่จ—่ฃฝ้€ ;; QMS/QSD

Dates and Status

Sep 18, 2020

Sep 18, 2025