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"Terumo" guide line - Taiwan Registration 60265c1012235b66d8395448cbdd01b0

Access comprehensive regulatory information for "Terumo" guide line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60265c1012235b66d8395448cbdd01b0 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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60265c1012235b66d8395448cbdd01b0
Registration Details
Taiwan FDA Registration: 60265c1012235b66d8395448cbdd01b0
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Device Details

"Terumo" guide line
TW: "ๆณฐ็ˆพ่Œ‚"ๅฐŽๅผ•ๅฐŽ็ทš
Risk Class 2

Registration Details

60265c1012235b66d8395448cbdd01b0

DHA00600839408

Company Information

Product Details

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

import

Dates and Status

Sep 08, 1997

Feb 09, 2029