Taiwan FDA registration ec3f2d7e3f67b484173503c6871e2b0e
"Venoscope" Neonatal Transilluminator (Non-Sterile)
TW: "凡諾普" 透照器 (未滅菌)
Taiwan·Risk Class 1·MD·VENOSCOPE, L.L.C.·Registered Oct 18, 2016 – Oct 18, 2021ExpiredRegistration details
- Analysis ID
- ec3f2d7e3f67b484173503c6871e2b0e
- License Form
- Ministry of Health Medical Device Import No. 017091
- Customs Code
- DHA09401709104
Company information
- Manufacturer
- VENOSCOPE, L.L.C.
- Manufacturer Country
- United States
- Authorized Representative
- LIFE SCIENCE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1945 transillumination
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 18, 2016
- Expiry Date
- Oct 18, 2021
About this record
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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