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"VERICOM" General purpose disinfectants (non-sterile) - Taiwan Registration 05736fdb5b99d76ea9718966cffcc0c4

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.

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05736fdb5b99d76ea9718966cffcc0c4
Registration Details
Taiwan FDA Registration: 05736fdb5b99d76ea9718966cffcc0c4
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Device Details

"VERICOM" General purpose disinfectants (non-sterile)
TW: "่‘ณ็ˆพๅบท" ไธ€่ˆฌ้†ซ็™‚ๅ™จๆขฐ็”จๆถˆๆฏ’ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

05736fdb5b99d76ea9718966cffcc0c4

Ministry of Health Medical Device Import No. 013999

DHA09401399900

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".

J General hospital and personal use equipment

J6890 Disinfectants for general medical devices

Imported from abroad

Dates and Status

Mar 31, 2014

Mar 31, 2024