Taiwan FDA registration 133051ae2410f796181b5b9eade24649

"BenQ Santoyo" shadowless surgical light

TW: “明基三豐”無影外科手術燈
Taiwan flagTaiwan·Risk Class 2·BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory·Registered Apr 01, 2013 – Apr 01, 2018Cancelled
Registration details
Analysis ID
133051ae2410f796181b5b9eade24649
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)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4580 Surgical lamp
Import Information
Domestic
Dates and status
Registration Date
Apr 01, 2013
Expiry Date
Apr 01, 2018
Cancellation Date
Feb 26, 2019
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "BenQ Santoyo" shadowless surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 133051ae2410f796181b5b9eade24649 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, 2 companies making similar products including BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory, BENQ MEDICAL TECHNOLOGY CORPORATION, and 2 recent registrations in the same category. 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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