Taiwan FDA registration 0adcea87065426373d976964ae9972ff
“BenQ” Mercury Dental Implant Planning Software
TW: “明基三豐”植牙規劃軟體
Taiwan·Risk Class 2·MD·BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory·Registered May 01, 2019 – May 01, 2024ExpiredRegistration details
- Analysis ID
- 0adcea87065426373d976964ae9972ff
- License Form
- Ministry of Health Medical Device Manufacturing No. 006412
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 01, 2019
- Expiry Date
- May 01, 2024
About this record
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.
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