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"Toyobo" urine sediment quality solution (unsterilized) - Taiwan Registration 00a76e90446a2a24a0ac772ab503c3ba

Access comprehensive regulatory information for "Toyobo" urine sediment quality 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 00a76e90446a2a24a0ac772ab503c3ba and manufactured by TOYOBO CO., LTD.. The authorized representative in Taiwan is AMESDATA BIOTECH CO., 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.

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00a76e90446a2a24a0ac772ab503c3ba
Registration Details
Taiwan FDA Registration: 00a76e90446a2a24a0ac772ab503c3ba
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Device Details

"Toyobo" urine sediment quality solution (unsterilized)
TW: โ€œๆฑๆด‹็ดกโ€ๅฐฟๆฒ‰ๆธฃๅ“็ฎกๆถฒ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

00a76e90446a2a24a0ac772ab503c3ba

DHA04401229400

Company Information

Japan

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

Oct 23, 2012

Oct 23, 2027