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“BenQ” Mercury Dental Implant Planning Software - Taiwan Registration 0adcea87065426373d976964ae9972ff

Access comprehensive regulatory information for “BenQ” Mercury Dental Implant Planning Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0adcea87065426373d976964ae9972ff and manufactured by BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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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0adcea87065426373d976964ae9972ff
Registration Details
Taiwan FDA Registration: 0adcea87065426373d976964ae9972ff
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Device Details

“BenQ” Mercury Dental Implant Planning Software
TW: “明基三豐”植牙規劃軟體
Risk Class 2
MD

Registration Details

0adcea87065426373d976964ae9972ff

Ministry of Health Medical Device Manufacturing No. 006412

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P2050 Medical Image Management and Processing System

Produced in Taiwan, China

Dates and Status

May 01, 2019

May 01, 2024