Taiwan FDA registration 74919f2db5589cce175d1e5ac8fc3730

"Mitoyo" total reflection shadowless surgical light

TW: "三豐"全反射無影手術燈
Taiwan flagTaiwan·Risk Class 2·Mitutoyo Medical Equipment Co., Ltd·Registered Jan 02, 2007 – Jan 02, 2017Cancelled
Registration details
Analysis ID
74919f2db5589cce175d1e5ac8fc3730
Customs Code
DHY00500211601
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
Jan 02, 2007
Expiry Date
Jan 02, 2017
Cancellation Date
Feb 27, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期;;自請註銷
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About this record

Access comprehensive regulatory information for "Mitoyo" total reflection 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 74919f2db5589cce175d1e5ac8fc3730 and manufactured by Mitutoyo Medical Equipment Co., Ltd. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BENQ MEDICAL TECHNOLOGY CORPORATION, and 1 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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