Pure Global

VIROTROL Syphilis LR-A - Taiwan Registration d95258b09fda96f2f4b30ed3d9490986

Access comprehensive regulatory information for VIROTROL Syphilis LR-A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d95258b09fda96f2f4b30ed3d9490986 and manufactured by BIO-RAD LABORATORIES. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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 Database
Powered by Pure Global AI
89,000+ Devices
d95258b09fda96f2f4b30ed3d9490986
Registration Details
Taiwan FDA Registration: d95258b09fda96f2f4b30ed3d9490986
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

VIROTROL Syphilis LR-A
TW: ๅจๆจ‚ๆบ– ๆข…ๆฏ’ๅ“็ฎกๆถฒ
Risk Class 2
MD

Registration Details

d95258b09fda96f2f4b30ed3d9490986

Ministry of Health Medical Device Import No. 029586

DHA05602958601

Company Information

United States

Product Details

This product is an unanalyzed precision quality control solution, which can be used as an in vitro diagnostic analysis procedure for qualitative determination of Treponema pallidum antibodies. This product can be used as a tool to estimate precision and can be used to detect systematic deviations in specific laboratory test procedures.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Jun 22, 2017

Jun 22, 2027