Taiwan FDA registration a93bb906715c489ce337ee66c594478c

"Weigang" bone cement mixer (unsterilized)

TW: “維綱”骨水泥攪拌器 (未滅菌)

Taiwan·Risk Class 1·Weigang Biotechnology Co., Ltd. Triple Second Factory·Registered Jan 07, 2010 – Jan 07, 2015Cancelled

Registration details

Analysis ID: a93bb906715c489ce337ee66c594478c

Company information

Manufacturer: Weigang Biotechnology Co., Ltd. Triple Second Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOTECH ONE INC.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Clinical Bone Cement Mixer (N.4210)".
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4210 臨床用骨水泥攪拌器
Import Information: Domestic

Dates and status

Registration Date: Jan 07, 2010
Expiry Date: Jan 07, 2015
Cancellation Date: Jun 08, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Weigang" bone cement mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a93bb906715c489ce337ee66c594478c and manufactured by Weigang Biotechnology Co., Ltd. Triple Second Factory. The authorized representative in Taiwan is BIOTECH ONE INC..

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