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"Instrument Lab" quality control solution (unsterilized) - Taiwan Registration 91951a89b452733eb030498463dd09e4

Access comprehensive regulatory information for "Instrument Lab" quality control solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91951a89b452733eb030498463dd09e4 and manufactured by INSTRUMENTATION LABORATORY CO.,. The authorized representative in Taiwan is Werfen Taiwan Limited.

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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91951a89b452733eb030498463dd09e4
Registration Details
Taiwan FDA Registration: 91951a89b452733eb030498463dd09e4
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Device Details

"Instrument Lab" quality control solution (unsterilized)
TW: โ€œๅ„€ๅ™จๅฏฆ้ฉ—ๅฎคโ€ๅ“็ฎกๆถฒ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

91951a89b452733eb030498463dd09e4

DHA04400546500

Company Information

United States

Product Details

Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

import

Dates and Status

Dec 21, 2006

Dec 21, 2026