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"Venoscope" Neonatal Transilluminator (Non-Sterile) - Taiwan Registration ec3f2d7e3f67b484173503c6871e2b0e

Access comprehensive regulatory information for "Venoscope" Neonatal Transilluminator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec3f2d7e3f67b484173503c6871e2b0e and manufactured by VENOSCOPE, L.L.C.. The authorized representative in Taiwan is LIFE SCIENCE CO., LTD..

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ec3f2d7e3f67b484173503c6871e2b0e
Registration Details
Taiwan FDA Registration: ec3f2d7e3f67b484173503c6871e2b0e
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Device Details

"Venoscope" Neonatal Transilluminator (Non-Sterile)
TW: "ๅ‡ก่ซพๆ™ฎ" ้€็…งๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ec3f2d7e3f67b484173503c6871e2b0e

Ministry of Health Medical Device Import No. 017091

DHA09401709104

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".

M Ophthalmic devices

M1945 transillumination

Imported from abroad

Dates and Status

Oct 18, 2016

Oct 18, 2021