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"AGRA" osmotic analyzer (unsterilized) - Taiwan Registration edcbd2774e12717b36d24435ea10fd62

Access comprehensive regulatory information for "AGRA" osmotic analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number edcbd2774e12717b36d24435ea10fd62 and manufactured by ARKRAY FACTORY, INC.. The authorized representative in Taiwan is MEDTRI 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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edcbd2774e12717b36d24435ea10fd62
Registration Details
Taiwan FDA Registration: edcbd2774e12717b36d24435ea10fd62
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Device Details

"AGRA" osmotic analyzer (unsterilized)
TW: "ๆ„›็ง‘ไพ†" ๆปฒ้€ๅฃ“ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

edcbd2774e12717b36d24435ea10fd62

DHA09401694808

Company Information

Japan

Product Details

It is limited to the first level identification scope of the permeameter (A.2730) for clinical use.

A Clinical chemistry and clinical toxicology

A.2730 Permeameter for clinical use

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Aug 31, 2016

Aug 31, 2026