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Anminine rupture of membranes (placental microglobulin) detector (sterilization) - Taiwan Registration a1033f2eab4206f9fc1d2a11b189bcec

Access comprehensive regulatory information for Anminine rupture of membranes (placental microglobulin) detector (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1033f2eab4206f9fc1d2a11b189bcec and manufactured by QIAGEN. The authorized representative in Taiwan is A-STRONG 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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a1033f2eab4206f9fc1d2a11b189bcec
Registration Details
Taiwan FDA Registration: a1033f2eab4206f9fc1d2a11b189bcec
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Device Details

Anminine rupture of membranes (placental microglobulin) detector (sterilization)
TW: ใ€ๅฎ‰ๆ•ๅฏงใ€ž่ƒŽ่†œ็ ด่ฃ‚(่ƒŽ็›คๅพฎ็ƒ่›‹็™ฝ)ๆชขๆธฌๅŠ‘(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a1033f2eab4206f9fc1d2a11b189bcec

DHA04401115405

Company Information

United States

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Uric pH (Non-quantitative) Test System (A.1550)".

A Clinical chemistry and clinical toxicology

A.1550 Uric pH (non-quantitative) testing system

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 07, 2011

Dec 07, 2021

Sep 23, 2023

Cancellation Information

Logged out

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