Taiwan FDA registration 05736fdb5b99d76ea9718966cffcc0c4

"VERICOM" General purpose disinfectants (non-sterile)

TW: "葳爾康" 一般醫療器械用消毒劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·VERICOM CO., LTD.·Registered Mar 31, 2014 – Mar 31, 2024Expired
Registration details
Analysis ID
05736fdb5b99d76ea9718966cffcc0c4
License Form
Ministry of Health Medical Device Import No. 013999
Customs Code
DHA09401399900
Company information
Manufacturer
VERICOM CO., LTD.
Manufacturer Country
Korea, Republic of
Authorized Representative
SUNDENT CORPORATION
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6890 Disinfectants for general medical devices
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 31, 2014
Expiry Date
Mar 31, 2024
About this record

Access comprehensive regulatory information for "VERICOM" General purpose disinfectants (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 05736fdb5b99d76ea9718966cffcc0c4 and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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