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"Hanyang" low ion buffer solution (unsterilized) - Taiwan Registration a5bc5fb8a1a2379cdf45e8fdbc89752a

Access comprehensive regulatory information for "Hanyang" low ion buffer 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 a5bc5fb8a1a2379cdf45e8fdbc89752a and manufactured by METEK LAB INC.. The authorized representative in Taiwan is METEK LAB INC..

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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a5bc5fb8a1a2379cdf45e8fdbc89752a
Registration Details
Taiwan FDA Registration: a5bc5fb8a1a2379cdf45e8fdbc89752a
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Device Details

"Hanyang" low ion buffer solution (unsterilized)
TW: โ€œ็€šๆšโ€ ไฝŽ้›ขๅญ็ทฉ่กๆบถๆถฒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a5bc5fb8a1a2379cdf45e8fdbc89752a

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, in vitro diagnostic intensive medium (B.9600) first level identification range.

B Hematology, pathology, and genetics

B.9600 Intensive medium for in vitro diagnostics

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Aug 24, 2021

Aug 24, 2026