Taiwan FDA registration a4beffba969f239a73ee091080abdfe5

"Kashiwa Riki" bone water mud distributor (sterilization)

TW: “柏力”骨水泥分配器 (滅菌)

Taiwan·Risk Class 1·Heqi Biotechnology Co., Ltd.;; Baili Technology Co., Ltd·Registered Jun 29, 2021 – Jun 29, 2026Expired

Registration details

Analysis ID: a4beffba969f239a73ee091080abdfe5

Company information

Manufacturer: Heqi Biotechnology Co., Ltd.;; Baili Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOLIFE MEDICAL DEVICE INC.

Product details

Intended Use: Limited to the classification and grading management measures of medical equipment "Bone cement dispenser (N.4200) first level identification range.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4200 Bone cement distributor
Import Information: QMS/QSD;; 國產;; 委託製造

Dates and status

Registration Date: Jun 29, 2021
Expiry Date: Jun 29, 2026

About this record

Access comprehensive regulatory information for "Kashiwa Riki" bone water mud distributor (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4beffba969f239a73ee091080abdfe5 and manufactured by Heqi Biotechnology Co., Ltd.;; Baili Technology Co., Ltd. The authorized representative in Taiwan is BIOLIFE MEDICAL DEVICE INC..

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.