Taiwan FDA registration 95671790540759bcd6624bd7ca0a53d9

Vinosco vascular transilluminator (unsterilized)

TW: “維諾斯可”血管透照器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·VENOSCOPE, L.L.C.·Registered Feb 27, 2009 – Feb 27, 2019Cancelled
Registration details
Analysis ID
95671790540759bcd6624bd7ca0a53d9
Customs Code
DHA04400752502
Company information
Manufacturer
VENOSCOPE, L.L.C.
Manufacturer Country
United States
Authorized Representative
EVERMEDICAL COMPANY 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 Ophthalmology
Product Type (Level 2)
M.1945 Transilluminator
Import Information
import
Dates and status
Registration Date
Feb 27, 2009
Expiry Date
Feb 27, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for Vinosco vascular transilluminator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95671790540759bcd6624bd7ca0a53d9 and manufactured by VENOSCOPE, L.L.C.. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices