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"Terumo" leads for angiography - Taiwan Registration a19886920a4aba431c16ac3fc53b6ef5

Access comprehensive regulatory information for "Terumo" leads for angiography in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a19886920a4aba431c16ac3fc53b6ef5 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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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a19886920a4aba431c16ac3fc53b6ef5
Registration Details
Taiwan FDA Registration: a19886920a4aba431c16ac3fc53b6ef5
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Device Details

"Terumo" leads for angiography
TW: "ๆณฐ็ˆพ่Œ‚"่ก€็ฎกๆ”ๅฝฑ็”จๅฐŽ็ทš
Risk Class 2

Registration Details

a19886920a4aba431c16ac3fc53b6ef5

DHA00600736700

Company Information

Product Details

The details are as detailed as the approved copy of the imitation label

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

import

Dates and Status

Nov 30, 1994

Feb 09, 2029